2006 ICD-9-CM OFFICIAL CODES
DISEASES TABULAR LIST 14
ICDMENU


 
 
 14. CONGENITAL ANOMALIES (740-759)
 
  740 Anencephalus and similar anomalies
 
      740.0 Anencephalus
           Acrania
           Amyelencephalus
           Hemianencephaly
           Hemicephaly
 
      740.1 Craniorachischisis
 
      740.2 Iniencephaly
 
  741 Spina bifida
 
          Excludes: spina bifida occulta
(756.17)
 
 
     The following fifth-digit subclassification is for use with category 741:
 
     0 unspecified region
 
     1 cervical region
 
    2 dorsal (thoracic) region
 
     3 lumbar region
 
           741.0_ With hydrocephalus
                 Arnold-Chiari syndrome, type II
                 Chiari malformation, type II
                 Any condition classifiable to 741.9 with any condition
                 classifiable to 742.3
 
           741.9_ Without mention of hydrocephalus
                Hydromeningocele (spinal)
                 Hydromyelocele
                Meningocele (spinal)
                 Meningomyelocele
                 Myelocele
                 Myelocystocele
                 Rachischisis
                Spina bifida (aperta)
                 Syringomyelocele
 
  742 Other congenital anomalies of nervous system
 
          Excludes: congenital central alveolar hypoventilation syndrome
(327.25)
 
      742.0 Encephalocele
           Encephalocystocele
           Encephalomyelocele
           Hydroencephalocele
           Hydromeningocele, cranial
           Meningocele, cerebral
           Meningoencephalocele
 
      742.1 Microcephalus
           Hydromicrocephaly
           Micrencephaly
 
      742.2 Reduction deformities of brain
           Absence of part of brain
           Agenesis of part of brain
           Agyria
           Aplasia of part of brain
           Arhinencephaly
           Holoprosencephaly
           Hypoplasia of part of brain
           Microgyria
 
      742.3 Congenital hydrocephalus
           Aqueduct of Sylvius:
           anomaly
           obstruction, congenital
           stenosis
           Atresia of foramina of Magendie and Luschka
           Hydrocephalus in newborn
 
           Excludes: hydrocephalus:
                    acquired
(331.3-331.4)
                    due to congenital toxoplasmosis (771.2)
                    with any condition classifiable to 741.9 (741.0)
 
      742.4 Other specified anomalies of brain
           Congenital cerebral cyst
           Macroencephaly
           Macrogyria
           Megalencephaly
           Multiple anomalies of brain NOS
           Porencephaly
           Ulegyria
 
      742.5 Other specified anomalies of spinal cord
 
           742.51 Diastematomyelia
 
           742.53 Hydromyelia
                 Hydrorhachis
 
           742.59 Other
                 Amyelia
                 Atelomyelia
                 Congenital anomaly of spinal meninges
                 Defective development of cauda equina
                 Hypoplasia of spinal cord
                 Myelatelia
                 Myelodysplasia
 
      742.8 Other specified anomalies of nervous system
           Agenesis of nerve
           Displacement of brachial plexus
           Familial dysautonomia
           Jaw-winking syndrome
           Marcus-Gunn syndrome
           Riley-Day syndrome
 
          Excludes: neurofibromatosis
(237.7)
 
      742.9 Unspecified anomaly of brain, spinal cord, and nervous system
           Anomaly of brain, nervous system, and spinal cord
           Congenital, of brain, nervous system, and spinal cord:
           disease of brain, nervous system, and spinal cord
           lesion of brain, nervous system, and spinal cord
           Deformity of brain, nervous system, and spinal cord
 
  743 Congenital anomalies of eye
 
      743.0 Anophthalmos
 
           743.00 Clinical anophthalmos, unspecified
                 Agenesis
                 Congenital absence of eye
                 Anophthalmos NOS
 
           743.03 Cystic eyeball, congenital
 
           743.06 Cryptophthalmos
 
      743.1 Microphthalmos
           Dysplasia of eye
           Hypoplasia of eye
           Rudimentary eye
 
           743.10 Microphthalmos, unspecified
 
           743.11 Simple microphthalmos
 
           743.12 Microphthalmos associated with other anomalies of eye and adnexa
 
      743.2 Buphthalmos
           Glaucoma:
           congenital
           newborn
           Hydrophthalmos
 
          Excludes: glaucoma of childhood
(365.14)
                    traumatic glaucoma due to birth injury (767.8)
 
           743.20 Buphthalmos, unspecified
 
           743.21 Simple buphthalmos
 
           743.22 Buphthalmos associated with other ocular anomalies
                 Keratoglobus, congenital, associated with buphthalmos
                 Megalocornea associated with buphthalmos
 
      743.3 Congenital cataract and lens anomalies
 
          Excludes: infantile cataract
(366.00-366.09)
 
           743.30 Congenital cataract, unspecified
 
           743.31 Capsular and subcapsular cataract
 
           743.32 Cortical and zonular cataract
 
           743.33 Nuclear cataract
 
           743.34 Total and subtotal cataract, congenital
 
           743.35 Congenital aphakia
                 Congenital absence of lens
 
           743.36 Anomalies of lens shape
                 Microphakia
                 Spherophakia
 
           743.37 Congenital ectopic lens
 
           743.39 Other
 
      743.4 Coloboma and other anomalies of anterior segment
 
           743.41 Anomalies of corneal size and shape
                 Microcornea
 
          Excludes: that associated with buphthalmos
(743.22)
 
           743.42 Corneal opacities, interfering with vision, congenital
 
           743.43 Other corneal opacities, congenital
 
           743.44 Specified anomalies of anterior chamber, chamber angle, and
                 related structures
                 Anomaly:
                 Axenfeld's
                 Peters'
                 Rieger's
 
           743.45 Aniridia
 
           743.46 Other specified anomalies of iris and ciliary body
                 Anisocoria, congenital
                 Atresia of pupil
                 Coloboma of iris
                 Corectopia
 
           743.47 Specified anomalies of sclera
 
           743.48 Multiple and combined anomalies of anterior segment
 
           743.49 Other
 
      743.5 Congenital anomalies of posterior segment
 
           743.51 Vitreous anomalies
                 Congenital vitreous opacity
 
           743.52 Fundus coloboma
 
           743.53 Chorioretinal degeneration, congenital
 
           743.54 Congenital folds and cysts of posterior segment
 
           743.55 Congenital macular changes
 
           743.56 Other retinal changes, congenital
 
           743.57 Specified anomalies of optic disc
                Coloboma of optic disc (congenital)
 
           743.58 Vascular anomalies
                 Congenital retinal aneurysm
 
           743.59 Other
 
      743.6 Congenital anomalies of eyelids, lacrimal system, and orbit
 
           743.61 Congenital ptosis
 
           743.62 Congenital deformities of eyelids
                 Ablepharon
                 Absence of eyelid
                 Accessory eyelid
                 Congenital:
                 ectropion
                 entropion
 
           743.63 Other specified congenital anomalies of eyelid
                 Absence, agenesis, of cilia
 
           743.64 Specified congenital anomalies of lacrimal gland
 
           743.65 Specified congenital anomalies of lacrimal passages
                 Absence, agenesis of:
                 lacrimal apparatus
                 punctum lacrimale
                 Accessory lacrimal canal
 
           743.66 Specified congenital anomalies of orbit
 
           743.69 Other
                 Accessory eye muscles
 
      743.8 Other specified anomalies of eye
 
          Excludes: congenital nystagmus
(379.51)
                    ocular albinism (270.2)
                    retinitis pigmentosa (362.74)
 
      743.9 Unspecified anomaly of eye
           Congenital:
           anomaly NOS of eye [any part]
           deformity NOS of eye [any part]
 
  744 Congenital anomalies of ear, face, and neck
 
           Excludes: anomaly of:
                    cervical spine
(754.2, 756.10-756.19)
                    larynx (748.2-748.3)
                    nose (748.0-748.1)
                    parathyroid gland (759.2)
                    thyroid gland (759.2)
                    cleft lip (749.10-749.25)
 
      744.0 Anomalies of ear causing impairment of hearing
 
          Excludes: congenital deafness without mention of cause
(380.0-389.9)
 
           744.00 Unspecified anomaly of ear with impairment of hearing
 
           744.01 Absence of external ear
                 Absence of:
                auditory canal (external)
                auricle (ear) (with stenosis or atresia of auditory canal)
 
           744.02 Other anomalies of external ear with impairment of hearing
                Atresia or stricture of auditory canal (external)
 
           744.03 Anomaly of middle ear, except ossicles
                Atresia or stricture of osseous meatus (ear)
 
           744.04 Anomalies of ear ossicles
                 Fusion of ear ossicles
 
           744.05 Anomalies of inner ear
                 Congenital anomaly of:
                 membranous labyrinth
                 organ of Corti
 
           744.09 Other
                 Absence of ear, congenital
 
      744.1 Accessory auricle
           Accessory tragus
           Polyotia
           Preauricular appendage
           Supernumerary:
           ear
           lobule
 
      744.2 Other specified anomalies of ear
 
          Excludes: that with impairment of hearing
(744.00-744.09)
 
           744.21 Absence of ear lobe, congenital
 
           744.22 Macrotia
 
           744.23 Microtia
 
           744.24 Specified anomalies of Eustachian tube
                 Absence of Eustachian tube
 
           744.29 Other
                 Bat ear
                 Darwin's tubercle
                 Pointed ear
                 Prominence of auricle
                 Ridge ear
 
          Excludes: preauricular sinus
(744.46)
 
      744.3 Unspecified anomaly of ear
           Congenital:
           anomaly NOS of ear, NEC
           deformity NOS of ear, NEC
 
      744.4 Branchial cleft cyst or fistula; preauricular sinus
 
           744.41 Branchial cleft sinus or fistula
                 Branchial:
                sinus (external) (internal)
                 vestige
 
           744.42 Branchial cleft cyst
 
           744.43 Cervical auricle
 
           744.46 Preauricular sinus or fistula
 
           744.47 Preauricular cyst
 
           744.49 Other
                Fistula (of):
                 auricle, congenital
                 cervicoaural
 
      744.5 Webbing of neck
           Pterygium colli
 
      744.8 Other specified anomalies of face and neck
 
           744.81 Macrocheilia
                 Hypertrophy of lip, congenital
 
           744.82 Microcheilia
 
           744.83 Macrostomia
 
           744.84 Microstomia
 
           744.89 Other
 
          Excludes: congenital fistula of lip
(750.25)
                    musculoskeletal anomalies (754.0-754.1, 756.0)
 
      744.9 Unspecified anomalies of face and neck
           Congenital:
           anomaly NOS of face [any part] or neck [any part]
           deformity NOS of face [any part] or neck [any part]
 
  745 Bulbus cordis anomalies and anomalies of cardiac septal closure
 
      745.0 Common truncus
           Absent septum between aorta and pulmonary artery
          Communication (abnormal) between aorta and pulmonary artery
           Aortic septal defect
           Common aortopulmonary trunk
           Persistent truncus arteriosus
 
      745.1 Transposition of great vessels
 
           745.10 Complete transposition of great vessels
                 Transposition of great vessels:
                 NOS
                 classical
 
           745.11 Double outlet right ventricle
                 Dextratransposition of aorta
                 Incomplete transposition of great vessels
                 Origin of both great vessels from right ventricle
                 Taussig-Bing syndrome or defect
 
           745.12 Corrected transposition of great vessels
 
           745.19 Other
 
      745.2 Tetralogy of Fallot
           Fallot's pentalogy
           Ventricular septal defect with pulmonary stenosis or atresia,
           dextraposition of aorta, and hypertrophy of right ventricle
 
          Excludes: Fallot's triad
(746.09)
 
      745.3 Common ventricle
           Cor triloculare biatriatum
           Single ventricle
 
      745.4 Ventricular septal defect
           Eisenmenger's defect or complex
           Gerbode defect
           Interventricular septal defect
           Left ventricular-right atrial communication
           Roger's disease
 
          Excludes: common atrioventricular canal type
(745.69)
                    single ventricle (745.3)
 
      745.5 Ostium secundum type atrial septal defect
           Defect:
           atrium secundum
           fossa ovalis
           Lutembacher's syndrome
           Patent or persistent:
           foramen ovale
           ostium secundum
 
      745.6 Endocardial cushion defects
 
           745.60 Endocardial cushion defect, unspecified type
 
           745.61 Ostium primum defect
                 Persistent ostium primum
 
           745.69 Other
                 Absence of atrial septum
                 Atrioventricular canal type ventricular septal defect
                 Common atrioventricular canal
                 Common atrium
 
      745.7 Cor biloculare
           Absence of atrial and ventricular septa
 
      745.8 Other
 
      745.9 Unspecified defect of septal closure
           Septal defect NOS
 
  746 Other congenital anomalies of heart
 
          Excludes: endocardial fibroelastosis
(425.3)
 
      746.0 Anomalies of pulmonary valve
 
          Excludes: infundibular or subvalvular pulmonic stenosis
(746.83)
                    tetralogy of Fallot (745.2)
 
           746.00 Pulmonary valve anomaly, unspecified
 
           746.01 Atresia, congenital
                 Congenital absence of pulmonary valve
 
           746.02 Stenosis, congenital
 
           746.09 Other
                 Congenital insufficiency of pulmonary valve
                 Fallot's triad or trilogy
 
      746.1 Tricuspid atresia and stenosis, congenital
           Absence of tricuspid valve
 
      746.2 Ebstein's anomaly
 
      746.3 Congenital stenosis of aortic valve
           Congenital aortic stenosis
 
           Excludes: congenital:
                    subaortic stenosis
(746.81)
                    supravalvular aortic stenosis (747.22)
 
      746.4 Congenital insufficiency of aortic valve
           Bicuspid aortic valve
           Congenital aortic insufficiency
 
      746.5 Congenital mitral stenosis
           Fused commissure of mitral valve
           Parachute deformity of mitral valve
           Supernumerary cusps of mitral valve
 
      746.6 Congenital mitral insufficiency
 
      746.7 Hypoplastic left heart syndrome
           Atresia, or marked hypoplasia, of aortic orifice or valve, with
           hypoplasia of ascending aorta and defective development of left
          ventricle (with mitral valve atresia)
 
      746.8 Other specified anomalies of heart
 
           746.81 Subaortic stenosis
 
           746.82 Cor triatriatum
 
           746.83 Infundibular pulmonic stenosis
                 Subvalvular pulmonic stenosis
 
           746.84 Obstructive anomalies of heart, NEC
                 Uhl's disease
 
           746.85 Coronary artery anomaly
                 Anomalous origin or communication of coronary artery
                 Arteriovenous malformation of coronary artery
                 Coronary artery:
                 absence
                 arising from aorta or pulmonary trunk
                 single
 
           746.86 Congenital heart block
                 Complete or incomplete atrioventricular [AV] block
 
           746.87 Malposition of heart and cardiac apex
                 Abdominal heart
                 Dextrocardia
                 Ectopia cordis
                Levocardia (isolated)
                 Mesocardia
 
          Excludes: dextrocardia with complete transposition of viscera
(759.3)
 
           746.89 Other
                 Atresia of cardiac vein
                 Hypoplasia of cardiac vein
                 Congenital:
                 cardiomegaly
                 diverticulum, left ventricle
                 pericardial defect
 
      746.9 Unspecified anomaly of heart
           Congenital:
           anomaly of heart NOS
           heart disease NOS
 
  747 Other congenital anomalies of circulatory system
 
      747.0 Patent ductus arteriosus
           Patent ductus Botalli
           Persistent ductus arteriosus
 
      747.1 Coarctation of aorta
 
          747.10 Coarctation of aorta (preductal) (postductal)
                 Hypoplasia of aortic arch
 
           747.11 Interruption of aortic arch
 
      747.2 Other anomalies of aorta
 
           747.20 Anomaly of aorta, unspecified
 
           747.21 Anomalies of aortic arch
                 Anomalous origin, right subclavian artery
                 Dextraposition of aorta
                 Double aortic arch
                 Kommerell's diverticulum
                 Overriding aorta
                 Persistent:
                 convolutions, aortic arch
                 right aortic arch
                 Vascular ring
 
          Excludes: hypoplasia of aortic arch
(747.10)
 
           747.22 Atresia and stenosis of aorta
                 Absence of aorta
                 Aplasia of aorta
                 Hypoplasia of aorta
                 Stricture of aorta
                Supra (valvular)-aortic stenosis
 
          Excludes: congenital aortic (valvular) stenosis or stricture, so stated
                   
(746.3)
                    hypoplasia of aorta in hypoplastic left heart syndrome (746.7)
 
           747.29 Other
                 Aneurysm of sinus of Valsalva
                 Congenital:
                 aneurysm of aorta
                 dilation of aorta
 
      747.3 Anomalies of pulmonary artery
           Agenesis of pulmonary artery
           Anomaly of pulmonary artery
           Atresia of pulmonary artery
           Coarctation of pulmonary artery
           Hypoplasia of pulmonary artery
           Stenosis of pulmonary artery
           Pulmonary arteriovenous aneurysm
 
      747.4 Anomalies of great veins
 
           747.40 Anomaly of great veins, unspecified
                 Anomaly NOS of:
                 pulmonary veins
                 vena cava
 
           747.41 Total anomalous pulmonary venous connection
                 Total anomalous pulmonary venous return [TAPVR]:
                 subdiaphragmatic
                 supradiaphragmatic
 
           747.42 Partial anomalous pulmonary venous connection
                 Partial anomalous pulmonary venous return
 
           747.49 Other anomalies of great veins
                Absence of vena cava (inferior) (superior)
                Congenital stenosis of vena cava (inferior) (superior)
                 Persistent:
                 left posterior cardinal vein
                 left superior vena cava
                 Scimitar syndrome
                 Transposition of pulmonary veins NOS
 
      747.5 Absence or hypoplasia of umbilical artery
           Single umbilical artery
 
      747.6 Other anomalies of peripheral vascular system
           Absence of artery or vein, NEC
           Anomaly of artery or vein, NEC
           Atresia of artery or vein, NEC
          Arteriovenous aneurysm (peripheral)
           Arteriovenous malformation of the peripheral vascular system
           Congenital:
          aneurysm (peripheral)
           phlebectasia
           stricture, artery
           varix
           Multiple renal arteries
 
           Excludes: anomalies of:
                    cerebral vessels
(747.81)
                    pulmonary artery (747.3)
                    congenital retinal aneurysm (743.58)
                    hemangioma (228.00-228.09)
                    lymphangioma (228.1)
 
           747.60 Anomaly of the peripheral vascular system, unspecified site
 
           747.61 Gastrointestinal vessel anomaly
 
           747.62 Renal vessel anomaly
 
           747.63 Upper limb vessel anomaly
 
           747.64 Lower limb vessel anomaly
 
           747.69 Anomalies of other specified sites of peripheral vascular system
 
      747.8 Other specified anomalies of circulatory system
 
           747.81 Anomalies of cerebrovascular system
                 Arteriovenous malformation of brain
                 Cerebral arteriovenous aneurysm, congenital
                 Congenital anomalies of cerebral vessels
 
          Excludes: ruptured cerebral (arteriovenous) aneurysm (430)
 
           747.82 Spinal vessel anomaly
                 Arteriovenous malformation of spinal vessel
 
           747.83 Persistent fetal circulation
                 Persistent pulmonary hypertension
                 Primary pulmonary hypertension of newborn
 
           747.89 Other
                 Aneurysm, congenital, specified site not elsewhere classified
 
           Excludes: congenital aneurysm:
                    coronary
(746.85)
                    peripheral (747.6)
                    pulmonary (747.3)
                    retinal (743.58)
 
      747.9 Unspecified anomaly of circulatory system
 
  748 Congenital anomalies of respiratory system
 
          Excludes: congenital central alveolar hypoventilation syndrome
(327.25)
                    congenital defect of diaphragm (756.6)
 
      748.0 Choanal atresia
          Atresia of nares (anterior) (posterior)
          Congenital stenosis of nares (anterior) (posterior)
 
      748.1 Other anomalies of nose
           Absent nose
           Accessory nose
           Cleft nose
           Deformity of wall of nasal sinus
           Congenital:
           deformity of nose
           notching of tip of nose
           performation of wall of nasal sinus
 
          Excludes: congenital deviation of nasal septum
(754.0)
 
      748.2 Web of larynx
           Web of larynx:
           NOS
           glottic
           subglottic
 
      748.3 Other anomalies of larynx, trachea, and bronchus
           Absence or agenesis of:
           bronchus
           larynx
           trachea
          Anomaly (of):
           cricoid cartilage
           epiglottis
           thyroid cartilage
           tracheal cartilage
          Atresia (of):
           epiglottis
           glottis
           larynx
           trachea
           Cleft thyroid, cartilage, congenital
           Congenital:
           dilation, trachea
           stenosis:
           larynx
           trachea
           tracheocele
           Diverticulum:
           bronchus
           trachea
           Fissure of epiglottis
           Laryngocele
          Posterior cleft of cricoid cartilage (congenital)
           Rudimentary tracheal bronchus
           Stridor, laryngeal, congenital
 
      748.4 Congenital cystic lung
           Disease, lung:
           cystic, congenital
           polycystic, congenital
           Honeycomb lung, congenital
 
          Excludes: acquired or unspecified cystic lung
(518.89)
 
      748.5 Agenesis, hypoplasia, and dysplasia of lung
          Absence of lung (fissures) (lobe)
           Aplasia of lung
          Hypoplasia of lung (lobe)
           Sequestration of lung
 
      748.6 Other anomalies of lung
 
           748.60 Anomaly of lung, unspecified
 
           748.61 Congenital bronchiectasis
 
           748.69 Other
                Accessory lung (lobe)
                Azygos lobe (fissure), lung
 
      748.8 Other specified anomalies of respiratory system
           Abnormal communication between pericardial and pleural sacs
           Anomaly, pleural folds
           Atresia of nasopharynx
           Congenital cyst of mediastinum
 
      748.9 Unspecified anomaly of respiratory system
           Anomaly of respiratory system NOS
 
  749 Cleft palate and cleft lip
 
      749.0 Cleft palate
 
           749.00 Cleft palate, unspecified
 
           749.01 Unilateral, complete
 
           749.02 Unilateral, incomplete
                 Cleft uvula
 
           749.03 Bilateral, complete
 
           749.04 Bilateral, incomplete
 
      749.1 Cleft lip
           Cheiloschisis
           Congenital fissure of lip
           Harelip
           Labium leporinum
 
           749.10 Cleft lip, unspecified
 
           749.11 Unilateral, complete
 
           749.12 Unilateral, incomplete
 
           749.13 Bilateral, complete
 
           749.14 Bilateral, incomplete
 
      749.2 Cleft palate with cleft lip
           Cheilopalatoschisis
 
           749.20 Cleft palate with cleft lip, unspecified
 
           749.21 Unilateral, complete
 
           749.22 Unilateral, incomplete
 
           749.23 Bilateral, complete
 
           749.24 Bilateral, incomplete
 
           749.25 Other combinations
 
  750 Other congenital anomalies of upper alimentary tract
 
          Excludes: dentofacial anomalies
(524.0-524.9)
 
      750.0 Tongue tie
           Ankyloglossia
 
      750.1 Other anomalies of tongue
 
           750.10 Anomaly of tongue, unspecified
 
           750.11 Aglossia
 
           750.12 Congenital adhesions of tongue
 
           750.13 Fissure of tongue
                 Bifid tongue
                 Double tongue
 
           750.15 Macroglossia
                 Congenital hypertrophy of tongue
 
           750.16 Microglossia
                 Hypoplasia of tongue
 
           750.19 Other
 
      750.2 Other specified anomalies of mouth and pharynx
 
           750.21 Absence of salivary gland
 
           750.22 Accessory salivary gland
 
           750.23 Atresia, salivary gland
                 Imperforate salivary duct
 
           750.24 Congenital fistula of salivary gland
 
           750.25 Congenital fistula of lip
                Congenital (mucus) lip pits
 
           750.26 Other specified anomalies of mouth
                 Absence of uvula
 
           750.27 Diverticulum of pharynx
                 Pharyngeal pouch
 
           750.29 Other specified anomalies of pharynx
                 Imperforate pharynx
 
      750.3 Tracheoesophageal fistula, esophageal atresia and stenosis
           Absent esophagus
           Atresia of esophagus
           Congenital:
           esophageal ring
           stenosis of esophagus
           stricture of esophagus
           Congenital fistula:
           esophagobronchial
           esophagotracheal
           Imperforate esophagus
           Webbed esophagus
 
      750.4 Other specified anomalies of esophagus
           Dilatation, congenital, of esophagus
           Displacement, congenital, of esophagus
           Diverticulum of esophagus
           Duplication of esophagus
           Giant esophagus
           Esophageal pouch
 
          Excludes: congenital hiatus hernia
(750.6)
 
      750.5 Congenital hypertrophic pyloric stenosis
           Congenital or infantile:
           constriction of pylorus
           hypertrophy of pylorus
           spasm of pylorus
           stenosis of pylorus
           stricture of pylorus
 
      750.6 Congenital hiatus hernia
           Displacement of cardia through esophageal hiatus
 
          Excludes: congenital diaphragmatic hernia
(756.6)
 
      750.7 Other specified anomalies of stomach
           Congenital:
           cardiospasm
           hourglass stomach
           Displacement of stomach
           Diverticulum of stomach, congenital
           Duplication of stomach
           Megalogastria
           Microgastria
           Transposition of stomach
 
      750.8 Other specified anomalies of upper alimentary tract
 
      750.9 Unspecified anomaly of upper alimentary tract
           Congenital:
           anomaly NOS of upper alimentary tract [any part, except tongue]
           deformity NOS of upper alimentary tract [any part, except tongue]
 
  751 Other congenital anomalies of digestive system
 
      751.0 Meckel's diverticulum
          Meckel's diverticulum (displaced) (hypertrophic)
           Persistent:
           omphalomesenteric duct
           vitelline duct
 
      751.1 Atresia and stenosis of small intestine
           Atresia of:
           duodenum
           ileum
           intestine NOS
           Congenital:
           absence of small intestine or intestine NOS
           obstruction of small intestine or intestine NOS
           stenosis of small intestine or intestine NOS
           stricture of small intestine or intestine NOS
           Imperforate jejunum
 
      751.2 Atresia and stenosis of large intestine, rectum, and anal canal
           Absence:
          anus (congenital)
           appendix, congenital
           large instestine, congenital
           rectum
           Atresia of:
           anus
           colon
           rectum
           Congenital or infantile:
           obstruction of large intestine
           occlusion of anus
           stricture of anus
           Imperforate:
           anus
           rectum
           Stricture of rectum, congenital
 
      751.3 Hirschsprung's disease and other congenital functional disorders of
           colon
           Aganglionosis
           Congenital dilation of colon
           Congenital megacolon
           Marcrocolon
 
      751.4 Anomalies of intestinal fixation
           Congenital adhesions:
           omental, anomalous
           peritoneal
           Jackson's membrane
           Malrotation of colon
           Rotation of cecum or colon:
           failure of
           incomplete
           insufficient
           Universal mesentery
 
      751.5 Other anomalies of intestine
           Congenital diverticulum, colon
           Dolichocolon
           Duplication of:
           anus
           appendix
           cecum
           intestine
           Ectopic anus
           Megaloappendix
           Megaloduodenum
           Microcolon
           Persistent cloaca
           Transposition of:
           appendix
           colon
           intestine
 
      751.6 Anomalies of gallbladder, bile ducts, and liver
 
           751.60 Unspecified anomaly of gallbladder, bile ducts, and liver
 
           751.61 Biliary atresia
                 Congenital:
                absence of bile duct (common) or passage
                hypoplasia of bile duct (common) or passage
                obstruction of bile duct (common) or passage
                stricture of bile duct (common) or passage
 
           751.62 Congenital cystic disease of liver
                 Congenital polycystic disease of liver
                 Fibrocystic disease of liver
 
           751.69 Other anomalies of gallbladder, bile ducts, and liver
                 Absence of:
                 gallbladder, congenital
                liver (lobe)
                 Accessory:
                 hepatic ducts
                 liver
                 Congenital:
                 choledochal cyst
                 hepatomegaly
                 Duplication of:
                 biliary duct
                 cystic duct
                 gallbladder
                 liver
                 Floating:
                 gallbladder
                 liver
                 Intrahepatic gallbladder
 
      751.7 Anomalies of pancreas
           Absence of pancreas
           Accessory pancreas
           Agenesis of pancreas
           Annular pancreas
           Ectopic pancreatic tissue
           Hypoplasia of pancreas
           Pancreatic heterotopia
 
           Excludes: diabetes mellitus:
                    congenital
(250.0-250.9)
                    neonatal (775.1)
                    fibrocystic disease of pancreas (277.00-277.09)
 
      751.8 Other specified anomalies of digestive system
          Absence (complete) (partial) of alimentary tract NOS
           Duplication of digestive organs NOS
           Malposition, congenital of digestive organs NOS
 
          Excludes: congenital diaphragmatic hernia
(756.6)
                    congenital hiatus hernia (750.6)
 
      751.9 Unspecified anomaly of digestive system
           Congenital:
           anomaly NOS of digestive system NOS
           deformity NOS of digestive system NOS
 
  752 Congenital anomalies of genital organs
 
           Excludes: syndromes associated with anomalies in the number and form of
                    chromosomes
(758.0-758.9)
                    testicular feminization syndrome (259.5)
 
      752.0 Anomalies of ovaries
           Absence, congenital, of ovary
           Accessory ovary
           Ectopic ovary
           Streak of ovary
 
      752.1 Anomalies of fallopian tubes and broad ligaments
 
           752.10 Unspecified anomaly of fallopian tubes and broad ligaments
 
           752.11 Embryonic cyst of fallopian tubes and broad ligaments
                 Cyst:
                 epoophoron
                 fimbrial
                 parovarian
 
           752.19 Other
                 Absence of fallopian tube or broad ligament
                 Accessory fallopian tube or broad ligament
                 Atresia of fallopian tube or broad ligament
 
      752.2 Doubling of uterus
           Didelphic uterus
          Doubling of uterus [any degree] (associated with doubling of cervix and
           vagina)
 
      752.3 Other anomalies of uterus
           Absence, congenital, of uterus
           Agenesis of uterus
           Aplasia of uterus
           Bicornuate uterus
           Uterus unicornis
           Uterus with only one functioning horn
 
      752.4 Anomalies of cervix, vagina, and external female genitalia
 
           752.40 Unspecified anomaly of cervix, vagina, and external female
                 genitalia
 
           752.41 Embryonic cyst of cervix, vagina, and external female genitalia
                 Cyst of:
                 canal of Nuck, congenital
                 Gartner's duct
                 vagina, embryonal
                 vulva, congenital
 
           752.42 Imperforate hymen
 
           752.49 Other anomalies of cervix, vagina, and external female genitalia
                 Absence of cervix, clitoris, vagina, or vulva
                 Agenesis of cervix, clitoris, vagina, or vulva
                 Congenital stenosis or stricture of:
                 cervical canal
                 vagina
 
          Excludes: double vagina associated with total duplication
(752.2)
 
      752.5 Undescended and retractile testicle
 
           752.51 Undescended testis
                 Cryptorchism
                 Ectopic testis
 
           752.52 Retractile testis
 
      752.6 Hypospadias and epispadias and other penile anomalies
 
           752.61 Hypospadias
 
           752.62 Epispadias
                 Anaspadias
 
           752.63 Congenital chordee
 
           752.64 Micropenis
 
           752.65 Hidden penis
 
           752.69 Other penile anomalies
 
      752.7 Indeterminate sex and pseudohermaphroditism
           Gynandrism
           Hermaphroditism
           Ovotestis
          Pseudohermaphroditism (male) (female)
           Pure gonadal dysgenesis
 
           Excludes: pseudohermaphroditism:
                    female, with adrenocortical disorder
(255.2)
                    male, with gonadal disorder (257.8)
                    with specified chromosomal anomaly (758.0-758.9)
                    testicular feminization syndrome (259.5)
 
      752.8 Other specified anomalies of genital organs
 
          Excludes: congenital hydrocele
(778.6)
                    penile anomalies (752.61-752.69)
                    phimosis or paraphimosis (605)
 
           752.81 Scrotal transposition
 
           752.89 Other specified anomalies of genital organs
                 Absence of:
                 prostate
                 spermatic cord
                 vas deferens
                 Anorchism
                Aplasia (congenital) of:
                 prostate
                 round ligament
                 testicle
                 Atresia of:
                 ejaculatory duct
                 vas deferens
                 Fusion of testes
                 Hypoplasia of testis
                 Monorchism
                 Polyorchism
 
      752.9 Unspecified anomaly of genital organs
           Congenital:
           anomaly NOS of genital organ, NEC
           deformity NOS of genital organ, NEC
 
  753 Congenital anomalies of urinary system
 
      753.0 Renal agenesis and dysgenesis
           Atrophy of kidney:
           congenital
           infantile
          Congenital absence of kidney(s)
          Hypoplasia of kidney(s)
 
      753.1 Cystic kidney disease
 
          Excludes: acquired cyst of kidney
(593.2)
 
           753.10 Cystic kidney disease, unspecified
 
           753.11 Congenital single renal cyst
 
           753.12 Polycystic kidney, unspecified type
 
           753.13 Polycystic kidney, autosomal dominant
 
           753.14 Polycystic kidney, autosomal recessive
 
           753.15 Renal dysplasia
 
           753.16 Medullary cystic kidney
                 Nephronopthisis
 
           753.17 Medullary sponge kidney
 
           753.19 Other specified cystic kidney disease
                 Multicystic kidney
 
      753.2 Obstructive defects of renal pelvis and ureter
 
           753.20 Unspecified obstructive defect of renal pelvis and ureter
 
           753.21 Congenital obstruction of ureteropelvic junction
 
           753.22 Congenital obstruction of ureterovesical junction
                 Adynamic ureter
                 Congenital hydroureter
 
           753.23 Congenital ureterocele
 
           753.29 Other
 
      753.3 Other specified anomalies of kidney
           Accessory kidney
           Congenital:
           calculus of kidney
           displaced kidney
           Discoid kidney
           Double kidney with double pelvis
           Ectopic kidney
           Fusion of kidneys
           Giant kidney
           Horseshoe kidney
           Hyperplasia of kidney
           Lobulation of kidney
           Malrotation of kidney
          Trifid kidney (pelvis)
 
      753.4 Other specified anomalies of ureter
           Absent ureter
           Accessory ureter
           Deviaton of ureter
           Displaced ureteric orifice
           Double ureter
           Ectopic ureter
           Implantation, anomalous, of ureter
 
      753.5 Exstrophy of urinary bladder
           Ectopia vesicae
           Extroversion of bladder
 
      753.6 Atresia and stenosis of urethra and bladder neck
           Congenital obstruction:
           bladder neck
           urethra
           Congenital stricture of:
          urethra (valvular)
           urinary meatus
           vesicourethral orifice
           Imperforate urinary meatus
           Impervious urethra
           Urethral valve formation
 
      753.7 Anomalies of urachus
          Cyst (of) urachus
          Fistula (of) urachus
          Patent (of) urachus
           Persistent umbilical sinus
 
      753.8 Other specified anomalies of bladder and urethra
           Absence, congenital of:
           bladder
           urethra
           Accessory:
           bladder
           urethra
           Congenital:
           diverticulum of bladder
           hernia of bladder
           Congenital urethrorectal fistula
           Congenital prolapse of:
          bladder (mucosa)
           urethra
           Double:
           urethra
           urinary meatus
 
      753.9 Unspecified anomaly of urinary system
           Congenital:
           anomaly NOS of urinary system [any part, except urachus]
           deformity NOS of urinary system [any part, except urachus]
 
  754 Certain congenital musculoskeletal deformities
 
           Includes: nonteratogenic deformities which are considered to be due to
                     intrauterine malposition and pressure
 
      754.0 Of skull, face, and jaw
           Asymmetry of face
           Compression facies
           Depressions in skull
           Deviation of nasal septum, congenital
           Dolichocephaly
           Plagiocephaly
           Potter's facies
           Squashed or bent nose, congenital
 
          Excludes: dentofacial anomalies
(524.0-524.9)
                    syphilitic saddle nose (090.5)
 
      754.1 Of sternocleidomastoid muscle
           Congenital sternomastoid torticollis
           Congenital wryneck
          Contracture of sternocleidomastoid (muscle)
           Sternomastoid tumor
 
      754.2 Of spine
           Congenital postural:
           lordosis
           scoliosis
 
      754.3 Congenital dislocation of hip
 
           754.30 Congenital dislocation of hip, unilateral
                 Congenital dislocation of hip NOS
 
           754.31 Congenital dislocation of hip, bilateral
 
           754.32 Congenital subluxation of hip, unilateral
                 Congenital flexion deformity, hip or thigh
                 Predislocation status of hip at birth
                 Preluxation of hip, congenital
 
           754.33 Congenital subluxation of hip, bilateral
 
           754.35 Congenital dislocation of one hip with subluxation of other hip
 
      754.4 Congenital genu recurvatum and bowing of long bones of leg
 
           754.40 Genu recurvatum
 
          754.41 Congenital dislocation of knee (with genu recurvatum)
 
           754.42 Congenital bowing of femur
 
           754.43 Congenital bowing of tibia and fibula
 
           754.44 Congenital bowing of unspecified long bones of leg
 
      754.5 Varus deformities of feet
 
          Excludes: acquired
(736.71, 736.75, 736.79)
 
           754.50 Talipes varus
                 Congenital varus deformity of foot, unspecified
                 Pes varus
 
           754.51 Talipes equinovarus
                Equinovarus (congenital)
 
           754.52 Metatarsus primus varus
 
           754.53 Metatarsus varus
 
           754.59 Other
                 Talipes calcaneovarus
 
      754.6 Valgus deformities of feet
 
          Excludes: valgus deformity of foot (acquired) (736.79)
 
           754.60 Talipes valgus
                 Congenital valgus deformity of foot, unspecified
 
           754.61 Congenital pes planus
                 Congenital rocker bottom flat foot
                 Flat foot, congenital
 
          Excludes: pes planus (acquired) (734)
 
           754.62 Talipes calcaneovalgus
 
           754.69 Other
                 Talipes:
                 equinovalgus
                 planovalgus
 
      754.7 Other deformities of feet
 
          Excludes: acquired
(736.70-736.79)
 
           754.70 Talipes, unspecified
                 Congenital deformity of foot NOS
 
           754.71 Talipes cavus
                Cavus foot (congenital)
 
           754.79 Other
                 Asymmetric talipes
                 Talipes:
                 calcaneus
                 equinus
 
      754.8 Other specified nonteratogenic anomalies
 
           754.81 Pectus excavatum
                 Congenital funnel chest
 
           754.82 Pectus carinatum
                 Congenital pigeon chest [breast]
 
           754.89 Other
                Club hand (congenital)
                 Congenital:
                 deformity of chest wall
                 dislocation of elbow
                 Generalized flexion contractures of lower limb joints, congenital
                Spade-like hand (congenital)
 
  755 Other congenital anomalies of limbs
 
           Excludes: those deformities classifiable to 754.0-754.8
 
      755.0 Polydactyly
 
           755.00 Polydactyly, unspecified digits
                 Supernumerary digits
 
           755.01 Of fingers
                 Accessory fingers
 
           755.02 Of toes
                 Accessory toes
 
      755.1 Syndactyly
           Symphalangy
           Webbing of digits
 
           755.10 Of multiple and unspecified sites
 
           755.11 Of fingers without fusion of bone
 
           755.12 Of fingers with fusion of bone
 
           755.13 Of toes without fusion of bone
 
           755.14 Of toes with fusion of bone
 
      755.2 Reduction deformities of upper limb
 
           755.20 Unspecified reduction deformity of upper limb
                 Ectromelia NOS of upper limb
                 Hemimelia NOS of upper limb
                 Shortening of arm, congenital
 
           755.21 Transverse deficiency of upper limb
                 Amelia of upper limb
                 Congenital absence of:
                fingers, all (complete or partial)
                 forearm, including hand and fingers
                 upper limb, complete
                 Congenital amputation of upper limb
                 Transverse hemimelia of upper limb
 
           755.22 Longitudinal deficiency of upper limb, NEC
                 Phocomelia NOS of upper limb
                 Rudimentary arm
 
           755.23 Longitudinal deficiency, combined, involving humerus, radius,
                and ulna (complete or incomplete)
                Congenital absence of arm and forearm (complete or incomplete)
                 with or without metacarpal deficiency and/or phalangeal
                 deficiency, incomplete
                 Phocomelia, complete, of upper limb
 
          755.24 Longitudinal deficiency, humeral, complete or partial (with or
                 without distal deficiencies, incomplete)
                Congenital absence of humerus (with or without absence of some
                 [but not all] distal elements)
                 Proximal phocomelia of upper limb
 
          755.25 Longitudinal deficiency, radioulnar, complete or partial (with
                 or without distal deficiencies, incomplete)
                Congenital absence of radius and ulna (with or without absence of
                 some [but not all] distal elements)
                 Distal phocomelia of upper limb
 
          755.26 Longitudinal deficiency, radial, complete or partial (with or
                 without distal deficiencies, incomplete)
                 Agenesis of radius
                Congenital absence of radius (with or without absence of some
                 [but not all] distal elements)
 
          755.27 Longitudinal deficiency, ulnar, complete or partial (with or
                 without distal deficiencies, incomplete)
                 Agenesis of ulna
                Congenital absence of ulna (with or without absence of some [but
                 not all] distal elements)
 
           755.28 Longitudinal deficiency, carpals or metacarpals, complete or
                partial (with or without incomplete phalangeal deficiency)
 
           755.29 Longitudinal deficiency, phalanges, complete or partial
                 Absence of finger, congenital
                 Aphalangia of upper limb, terminal, complete or partial
 
          Excludes: terminal deficiency of all five digits
(755.21)
                    transverse deficiency of phalanges (755.21)
 
      755.3 Reduction deformities of lower limb
 
           755.30 Unspecified reduction deformity of lower limb
                 Ectromelia NOS of lower limb
                 Hemimelia NOS of lower limb
                 Shortening of leg, congenital
 
           755.31 Transverse deficiency of lower limb
                 Amelia of lower limb
                 Congenital absence of:
                 foot
                 leg, including foot and toes
                 lower limb, complete
                 toes, all, complete
                 Transverse hemimelia of lower limb
 
           755.32 Longitudinal deficiency of lower limb, NEC
                 Phocomelia NOS of lower limb
 
           755.33 Longitudinal deficiency, combined, involving femur, tibia, and
                fibula (complete or incomplete)
                Congenital absence of thigh and (lower) leg (complete or
                 incomplete) with or without metacarpal deficiency and/or
                 phalangeal deficiency, incomplete
                 Phocomelia, complete, of lower limb
 
          755.34 Longitudinal deficiency, femoral, complete or partial (with or
                 without distal deficiencies, incomplete)
                Congenital absence of femur (with or without absence of some [but
                 not all] distal elements)
                 Proximal phocomelia of lower limb
 
          755.35 Longitudinal deficiency, tibiofibular, complete or partial (with
                 or without distal deficiencies, incomplete)
                Congenital absence of tibia and fibula (with or without absence
                 of some [but not all] distal elements)
                 Distal phocomelia of lower limb
 
          755.36 Longitudinal deficiency, tibia, complete or partial (with or
                 without distal deficiencies, incomplete)
                 Agenesis of tibia
                Congenital absence of tibia (with or without absence of some [but
                 not all] distal elements)
 
          755.37 Longitudinal deficiency, fibular, complete or partial (with or
                 without distal deficiencies, incomplete)
                 Agenesis of fibula
                Congenital absence of fibula (with or without absence of some
                 [but not all] distal elements)
 
           755.38 Longitudinal deficiency, tarsals or metatarsals, complete or
                partial (with or without incomplete phalangeal deficiency)
 
           755.39 Longitudinal deficiency, phalanges, complete or partial
                 Absence of toe, congenital
                 Aphalangia of lower limb, terminal, complete or partial
 
          Excludes: terminal deficiency of all five digits
(755.31)
                    transverse deficiency of phalanges (755.31)
 
      755.4 Reduction deformities, unspecified limb
          Absence, congenital (complete or partial) of limb NOS
           Amelia of unspecified limb
           Ectromelia of unspecified limb
           Hemimelia of unspecified limb
           Phocomelia of unspecified limb
 
      755.5 Other anomalies of upper limb, including shoulder girdle
 
           755.50 Unspecified anomaly of upper limb
 
           755.51 Congenital deformity of clavicle
 
           755.52 Congenital elevation of scapula
                 Sprengel's deformity
 
           755.53 Radioulnar synostosis
 
           755.54 Madelung's deformity
 
           755.55 Acrocephalosyndactyly
                 Apert's syndrome
 
           755.56 Accessory carpal bones
 
          755.57 Macrodactylia (fingers)
 
           755.58 Cleft hand, congenital
                 Lobster-claw hand
 
           755.59 Other
                 Cleidocranial dysostosis
                 Cubitus:
                 valgus, congenital
                 varus, congenital
 
          Excludes: club hand (congenital) (754.89)
                    congenital dislocation of elbow
(754.89)
 
      755.6 Other anomalies of lower limb, including pelvic girdle
 
           755.60 Unspecified anomaly of lower limb
 
           755.61 Coxa valga, congenital
 
           755.62 Coxa vara, congenital
 
          755.63 Other congenital deformity of hip (joint)
                Congenital anteversion of femur (neck)
 
          Excludes: congenital dislocation of hip
(754.30-754.35)
 
          755.64 Congenital deformity of knee (joint)
                 Congenital:
                 absence of patella
                 genu valgum [knock-knee]
                 genu varum [bowleg]
                 Rudimentary patella
 
           755.65 Macrodactylia of toes
 
           755.66 Other anomalies of toes
                 Congenital:
                 hallux valgus
                 hallux varus
                 hammer toe
 
           755.67 Anomalies of foot, NEC
                 Astragaloscaphoid synostosis
                 Calcaneonavicular bar
                 Coalition of calcaneus
                 Talonavicular synostosis
                 Tarsal coalitions
 
           755.69 Other
                 Congenital:
                 angulation of tibia
                deformity (of):
                ankle (joint)
                sacroiliac (joint)
                 fusion of sacroiliac joint
 
      755.8 Other specified anomalies of unspecified limb
 
      755.9 Unspecified anomaly of unspecified limb
           Congenital:
           anomaly NOS of unspecified limb
           deformity NOS of unspecified limb
 
          Excludes: reduction deformity of unspecified limb
(755.4)
 
  756 Other congenital musculoskeletal anomalies
 
           Excludes: those deformities classifiable to 754.0-754.8
 
      756.0 Anomalies of skull and face bones
           Absence of skull bones
           Acrocephaly
           Congenital deformity of forehead
           Craniosynostosis
           Crouzon's disease
           Hypertelorism
           Imperfect fusion of skull
           Oxycephaly
           Platybasia
           Premature closure of cranial sutures
           Tower skull
           Trigonocephaly
 
          Excludes: acrocephalosyndactyly [Apert's syndrome]
(755.55)
                    dentofacial anomalies (524.0-524.9)
                     skull defects associated with brain anomalies, such as:
                    anencephalus (740.0)
                    encephalocele (742.0)
                    hydrocephalus (742.3)
                    microcephalus (742.1)
 
      756.1 Anomalies of spine
 
           756.10 Anomaly of spine, unspecified
 
           756.11 Spondylolysis, lumbosacral region
                Prespondylolisthesis (lumbosacral)
 
           756.12 Spondylolisthesis
 
           756.13 Absence of vertebra, congenital
 
           756.14 Hemivertebra
 
           756.15 Fusion of spine [vertebra], congenital
 
           756.16 Klippel-Feil syndrome
 
           756.17 Spina bifida occulta
 
          Excludes: spina bifida (aperta) (741.0-741.9)
 
           756.19 Other
                 Platyspondylia
                 Supernumerary vertebra
 
      756.2 Cervical rib
           Supernumerary rib in the cervical region
 
      756.3 Other anomalies of ribs and sternum
           Congenital absence of:
           rib
           sternum
           Congenital:
           fissure of sternum
           fusion of ribs
           Sternum bifidum
 
          Excludes: nonteratogenic deformity of chest wall
(754.81-754.89)
 
      756.4 Chondrodystrophy
           Achondroplasia
          Chondrodystrophia (fetalis)
           Dyschondroplasia
           Enchondromatosis
           Ollier's disease
 
          Excludes: lipochondrodystrophy [Hurler's syndrome]
(277.5)
                    Morquio's disease (277.5)
 
      756.5 Osteodystrophies
 
           756.50 Osteodystrophy, unspecified
 
           756.51 Osteogenesis imperfecta
                 Fragilitas ossium
                 Osteopsathyrosis
 
           756.52 Osteopetrosis
 
           756.53 Osteopoikilosis
 
           756.54 Polyostotic fibrous dysplasia of bone
 
           756.55 Chondroectodermal dysplasia
                 Ellis-van Creveld syndrome
 
           756.56 Multiple epiphyseal dysplasia
 
           756.59 Other
                Albright (-McCune)-Sternberg syndrome
 
      756.6 Anomalies of diaphragm
           Absence of diaphragm
           Congenital hernia:
           diaphragmatic
           foramen of Morgagni
           Eventration of diaphragm
 
          Excludes: congenital hiatus hernia
(750.6)
 
      756.7 Anomalies of abdominal wall
 
           756.70 Anomaly of abdominal wall, unspecified
 
           756.71 Prune belly syndrome
                 Eagle-Barrett syndrome
                 Prolapse of bladder mucosa
 
           756.79 Other congenital anomalies of abdominal wall
                 Exomphalos
                 Gastroschisis
                 Omphalocele
 
          Excludes umbilical hernia
(551-553 with .1)
 
      756.8 Other specified anomalies of muscle, tendon, fascia, and connective
           tissue
 
           756.81 Absence of muscle and tendon
                Absence of muscle (pectoral)
 
           756.82 Accessory muscle
 
           756.83 Ehlers-Danlos syndrome
 
           756.89 Other
                 Amyotrophia congenita
                 Congenital shortening of tendon
 
      756.9 Other and unspecified anomalies of musculoskeletal system
           Congenital:
           anomaly NOS of musculoskeletal system, NEC
           deformity NOS of musculoskeletal system, NEC
 
  757 Congenital anomalies of the integument
 
           Includes: anomalies of skin, subcutaneous tissue, hair, nails, and
                     breast
 
          Excludes: hemangioma
(228.00-228.09)
                    pigmented nevus (216.0-216.9)
 
      757.0 Hereditary edema of legs
           Congenital lymphedema
           Hereditary trophedema
           Milroy's disease
 
      757.1 Ichthyosis congenita
           Congenital ichthyosis
           Harlequin fetus
           Ichthyosiform erythroderma
 
      757.2 Dermatoglyphic anomalies
           Abnormal palmar creases
 
      757.3 Other specified anomalies of skin
 
           757.31 Congenital ectodermal dysplasia
 
           757.32 Vascular hamartomas
                 Birthmarks
                 Port-wine stain
                 Strawberry nevus
 
           757.33 Congenital pigmentary anomalies of skin
                 Congenital poikiloderma
                 Urticaria pigmentosa
                 Xeroderma pigmentosum
 
          Excludes: albinism
(270.2)
 
           757.39 Other
                 Accessory skin tags, congenital
                 Congenital scar
                 Epidermolysis bullosa
                Keratoderma (congenital)
 
          Excludes: pilonidal cyst
(685.0-685.1)
 
      757.4 Specified anomalies of hair
           Congenital:
           alopecia
           atrichosis
           beaded hair
           hypertrichosis
           monilethrix
           Persistent lanugo
 
      757.5 Specified anomalies of nails
           Anonychia
           Congenital:
           clubnail
           koilonychia
           leukonychia
           onychauxis
           pachyonychia
 
      757.6 Specified anomalies of breast
           Absent breast or nipple
           Accessory breast or nipple
           Supernumerary breast or nipple
           Hypoplasia of breast
 
          Excludes: absence of pectoral muscle
(756.81)
 
      757.8 Other specified anomalies of the integument
 
      757.9 Unspecified anomaly of the integument
           Congenital:
           anomaly NOS of integument
           deformity NOS of integument
 
  758 Chromosomal anomalies
 
           Includes: syndromes associated with anomalies in the number and form of
                     chromosomes
 
     Use additional codes for conditions associated with the chromosomal anomalies
 
      758.0 Down's syndrome
           Mongolism
           Translocation Down's syndrome
           Trisomy:
           21 or 22
           G
 
      758.1 Patau's syndrome
           Trisomy:
           13
           D1
 
      758.2 Edward's syndrome
           Trisomy:
           18
           E3
 
      758.3 Autosomal deletion syndromes
 
           758.31 Cri-du-chat syndrome
                 Deletion 5p
 
           758.32 Velo-cardio-facial syndrome
                 Deletion 22q11.2
 
           758.33 Other microdeletions
                 Miller-Dieker syndrome
                 Smith-Magenis syndrome
 
           758.39 Other autosomal deletions
 
      758.4 Balanced autosomal translocation in normal individual
 
      758.5 Other conditions due to autosomal anomalies
           Accessory autosomes NEC
 
      758.6 Gonadal dysgenesis
           Ovarian dysgenesis
           Turner's syndrome
           XO syndrome
 
          Excludes: pure gonadal dysgenesis
(752.7)
 
      758.7 Klinefelter's syndrome
           XXY syndrome
 
      758.8 Other conditions due to chromosome anomalies
 
           758.81 Other conditions due to sex chromosome anomalies
 
           758.89 Other
 
      758.9 Conditions due to anomaly of unspecified chromosome
 
  759 Other and unspecified congenital anomalies
 
      759.0 Anomalies of spleen
           Aberrant spleen
           Absent spleen
           Accessory spleen
           Congenital splenomegaly
           Ectopic spleen
           Lobulation of spleen
 
      759.1 Anomalies of adrenal gland
           Aberrant adrenal gland
           Absent adrenal gland
           Accessory adrenal gland
 
          Excludes: adrenogenital disorders
(255.2)
                    congenital disorders of steroid metabolism (255.2)
 
      759.2 Anomalies of other endocrine glands
           Absent parathyroid gland
           Accessory thyroid gland
           Persistent thyroglossal or thyrolingual duct
          Thyroglossal (duct) cyst
 
           Excludes: congenital:
                    goiter
(246.1)
                    hypothyroidism (243)
 
      759.3 Situs inversus
           Situs inversus or transversus:
           abdominalis
           thoracis
           Transposition of viscera:
           abdominal
           thoracic
 
           Excludes: dextrocardia without mention of complete transposition
                   
(746.87)
 
      759.4 Conjoined twins
           Craniopagus
           Dicephalus
           Pygopagus
           Thoracopagus
           Xiphopagus
 
      759.5 Tuberous sclerosis
           Bourneville's disease
           Epiloia
 
      759.6 Other hamartoses, NEC
           Syndrome:
           Peutz-Jeghers
          Sturge-Weber (-Dimitri)
           von Hippel-Lindau
 
          Excludes: neurofibromatosis
(237.7)
 
      759.7 Multiple congenital anomalies, so described
           Congenital:
           anomaly, multiple NOS
           deformity, multiple NOS
 
      759.8 Other specified anomalies
 
           759.81 Prader-Willi syndrome
 
           759.82 Marfan syndrome
 
           759.83 Fragile X syndrome
 
           759.89 Other
                 Congenital malformation syndromes affecting multiple systems, NEC
                 Laurence-Moon-Biedl syndrome
 
      759.9 Congenital anomaly, unspecified