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
- 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
- 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:
- 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
- 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:
- 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
- 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
- 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:
- 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
- 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:
- 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)
- 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
- 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
- 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
- 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
- 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
- 747.89 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 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
- 748.3 Other anomalies of larynx, trachea, and bronchus
- Absence or agenesis of:
- Anomaly (of):
- cricoid cartilage
- epiglottis
- thyroid cartilage
- tracheal cartilage
- Atresia (of):
- epiglottis
- glottis
- larynx
- trachea
- Cleft thyroid, cartilage, congenital
- Congenital:
- dilation, trachea
- stenosis:
- tracheocele
- Diverticulum:
- 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
- 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
- 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
- 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
- 750.27 Diverticulum of pharynx
- 750.29 Other specified anomalies of 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:
- Congenital or infantile:
- obstruction of large intestine
- occlusion of anus
- stricture of anus
- Imperforate:
- 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:
- 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:
- Congenital:
- choledochal cyst
- hepatomegaly
- Duplication of:
- biliary duct
- cystic duct
- gallbladder
- liver
- Floating:
- 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 (277.00-277.01)
- 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 (257.8)
- 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
- Gartner's duct
- 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
- 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:
- Excludes: double vagina associated with total duplication (752.2)
- 752.5 Undescended testicle
- Cryptorchism
- Ectopic testis
- 752.6 Hypospadias and epispadias
- Anaspadias
- Congenital chordee
- 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 (257.8)
- 752.8 Other specified anomalies of genital organs
- Absence of:
- penis
- prostate
- spermatic cord
- vas deferens
- Anorchism
- Aplasia (congenital) of:
- prostate
- round ligament
- testicle
- Atresia of:
- ejaculatory duct
- vas deferens
- Curvature of penis (lateral)
- Fusion of testes
- Hypoplasia of:
- Monorchism
- Paraspadias
- Polyorchism
- Excludes: congenital hydrocele (778.6)
- phimosis or paraphimosis (605)
- 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 absence of kidney(s)
- Hypoplasia of kidney(s)
- Code first any associated vesicoureteral reflux (593.70-593.73)
- 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
- Code first any associated vesicoureteral reflux (593.70-593.73)
- 753.16 Medullary cystic kidney
- 753.17 Medullary sponge kidney
- 753.19 Other specified cystic kidney disease
- 753.2 Obstructive defects of renal pelvis and ureter
- Atresia of ureter
- Congenital:
- dilatation of ureter
- hydronephrosis
- hydroureter
- megaloureter
- occlusion of ureter
- stricture of:
- ureter
- ureteropelvic junction
- ureterovesical orifice
- ureterocele
- Impervious ureter
- 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:
- 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:
- Accessory:
- Congenital:
- diverticulum of bladder
- hernia of bladder
- Congenital urethrorectal fistula
- Congenital prolapse of:
- Double:
- 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
- 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
- 754.52 Metatarsus primus varus
- 754.53 Metatarsus varus
- 754.59 Other
- 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
- 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
- 754.79 Other
- Asymmetric talipes
- Talipes:
- 754.8 Other specified nonteratogenic anomalies
- 754.81 Pectus excavatum
- 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
- 755.01 Of fingers
- 755.02 Of 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
- 755.53 Radioulnar synostosis
- 755.54 Madelung's deformity
- 755.55 Acrocephalosyndactyly
- 755.56 Accessory carpal bones
- 755.57 Macrodactylia (fingers)
- 755.58 Cleft hand, congenital
- 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:
- 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
- Exomphalos
- Gastroschisis
- Omphalocele
- Prune belly (syndrome)
- 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
- 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
- 758.0 Down's syndrome
- Mongolism
- Translocation Down's syndrome
- Trisomy:
- 758.1 Patau's syndrome
- 758.2 Edward's syndrome
- 758.3 Autosomal deletion syndromes
- Antimongolism syndrome
- Cri-du-chat syndrome
- 758.4 Balanced autosomal translocation in normal individual
- 758.5 Other conditions due to autosomal anomalies
- 758.6 Gonadal dysgenesis
- Ovarian dysgenesis
- Turner's syndrome
- XO syndrome
- Excludes: pure gonadal dysgenesis (752.7)
- 758.7 Klinefelter's syndrome
- 758.8 Other conditions due to sex chromosome anomalies
- Additional sex chromosome
- Sex chromosome mosaicism
- Syndrome:
- 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:
- Transposition of viscera:
- 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