Billable / specific codes

Chapter 17: Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders

• Q00.0Anencephaly
• Q00.1Craniorachischisis
• Q00.2Iniencephaly
• Q01.0Frontal encephalocele
• Q01.1Nasofrontal encephalocele
• Q01.2Occipital encephalocele
• Q01.8Encephalocele of other sites
• Q01.9Encephalocele, unspecified
• Q02Microcephaly
• Q03.0Malformations of aqueduct of Sylvius
• Q03.1Atresia of foramina of Magendie and Luschka
• Q03.8Other congenital hydrocephalus
• Q03.9Congenital hydrocephalus, unspecified
• Q04.0Congenital malformations of corpus callosum
• Q04.1Arhinencephaly
• Q04.2Holoprosencephaly
• Q04.3Other reduction deformities of brain
• Q04.4Septo-optic dysplasia of brain
• Q04.5Megalencephaly
• Q04.6Congenital cerebral cysts
• Q04.8Other specified congenital malformations of brain
• Q04.9Congenital malformation of brain, unspecified
• Q05.0Cervical spina bifida with hydrocephalus
• Q05.1Thoracic spina bifida with hydrocephalus
• Q05.2Lumbar spina bifida with hydrocephalus
• Q05.3Sacral spina bifida with hydrocephalus
• Q05.4Unspecified spina bifida with hydrocephalus
• Q05.5Cervical spina bifida without hydrocephalus
• Q05.6Thoracic spina bifida without hydrocephalus
• Q05.7Lumbar spina bifida without hydrocephalus
• Q05.8Sacral spina bifida without hydrocephalus
• Q05.9Spina bifida, unspecified
• Q06.0Amyelia
• Q06.1Hypoplasia and dysplasia of spinal cord
• Q06.2Diastematomyelia
• Q06.3Other congenital cauda equina malformations
• Q06.4Hydromyelia
• Q06.8Other specified congenital malformations of spinal cord
• Q06.9Congenital malformation of spinal cord, unspecified
• Q07.00Arnold-Chiari syndrome without spina bifida or hydrocephalus
• Q07.01Arnold-Chiari syndrome with spina bifida
• Q07.02Arnold-Chiari syndrome with hydrocephalus
• Q07.03Arnold-Chiari syndrome with spina bifida and hydrocephalus
• Q07.8Other specified congenital malformations of nervous system
• Q07.9Congenital malformation of nervous system, unspecified
• Q10.0Congenital ptosis
• Q10.1Congenital ectropion
• Q10.2Congenital entropion
• Q10.3Other congenital malformations of eyelid
• Q10.4Absence and agenesis of lacrimal apparatus
• Q10.5Congenital stenosis and stricture of lacrimal duct
• Q10.6Other congenital malformations of lacrimal apparatus
• Q10.7Congenital malformation of orbit
• Q11.0Cystic eyeball
• Q11.1Other anophthalmos
• Q11.2Microphthalmos
• Q11.3Macrophthalmos
• Q12.0Congenital cataract
• Q12.1Congenital displaced lens
• Q12.2Coloboma of lens
• Q12.3Congenital aphakia
• Q12.4Spherophakia
• Q12.8Other congenital lens malformations
• Q12.9Congenital lens malformation, unspecified
• Q13.0Coloboma of iris
• Q13.1Absence of iris
• Q13.2Other congenital malformations of iris
• Q13.3Congenital corneal opacity
• Q13.4Other congenital corneal malformations
• Q13.5Blue sclera
• Q13.81Rieger anomaly
• Q13.89Other congenital malformations of anterior segment of eye
• Q13.9Congenital malformation of anterior segment of eye, unspecified
• Q14.0Congenital malformation of vitreous humor
• Q14.1Congenital malformation of retina
• Q14.2Congenital malformation of optic disc
• Q14.3Congenital malformation of choroid
• Q14.8Other congenital malformations of posterior segment of eye
• Q14.9Congenital malformation of posterior segment of eye, unspecified
• Q15.0Congenital glaucoma
• Q15.8Other specified congenital malformations of eye
• Q15.9Congenital malformation of eye, unspecified
• Q16.0Congenital absence of (ear) auricle
• Q16.1Congenital absence, atresia and stricture of auditory canal (external)
• Q16.2Absence of eustachian tube
• Q16.3Congenital malformation of ear ossicles
• Q16.4Other congenital malformations of middle ear
• Q16.5Congenital malformation of inner ear
• Q16.9Congenital malformation of ear causing impairment of hearing, unspecified
• Q17.0Accessory auricle
• Q17.1Macrotia
• Q17.2Microtia
• Q17.3Other misshapen ear
• Q17.4Misplaced ear
• Q17.5Prominent ear
• Q17.8Other specified congenital malformations of ear
• Q17.9Congenital malformation of ear, unspecified
• Q18.0Sinus, fistula and cyst of branchial cleft
• Q18.1Preauricular sinus and cyst
• Q18.2Other branchial cleft malformations
• Q18.3Webbing of neck
• Q18.4Macrostomia
• Q18.5Microstomia
• Q18.6Macrocheilia
• Q18.7Microcheilia
• Q18.8Other specified congenital malformations of face and neck
• Q18.9Congenital malformation of face and neck, unspecified
• Q20.0Common arterial trunk
• Q20.1Double outlet right ventricle
• Q20.2Double outlet left ventricle
• Q20.3Discordant ventriculoarterial connection
• Q20.4Double inlet ventricle
• Q20.5Discordant atrioventricular connection
• Q20.6Isomerism of atrial appendages
• Q20.8Other congenital malformations of cardiac chambers and connections
• Q20.9Congenital malformation of cardiac chambers and connections, unspecified
• Q21.0Ventricular septal defect
• Q21.10Atrial septal defect, unspecified
• Q21.11Secundum atrial septal defect
• Q21.12Patent foramen ovale
• Q21.13Coronary sinus atrial septal defect
• Q21.14Superior sinus venosus atrial septal defect
• Q21.15Inferior sinus venosus atrial septal defect
• Q21.16Sinus venosus atrial septal defect, unspecified
• Q21.19Other specified atrial septal defect
• Q21.20Atrioventricular septal defect, unspecified as to partial or complete
• Q21.21Partial atrioventricular septal defect
• Q21.22Transitional atrioventricular septal defect
• Q21.23Complete atrioventricular septal defect
• Q21.3Tetralogy of Fallot
• Q21.4Aortopulmonary septal defect
• Q21.8Other congenital malformations of cardiac septa
• Q21.9Congenital malformation of cardiac septum, unspecified
• Q22.0Pulmonary valve atresia
• Q22.1Congenital pulmonary valve stenosis
• Q22.2Congenital pulmonary valve insufficiency
• Q22.3Other congenital malformations of pulmonary valve
• Q22.4Congenital tricuspid stenosis
• Q22.5Ebstein's anomaly
• Q22.6Hypoplastic right heart syndrome
• Q22.8Other congenital malformations of tricuspid valve
• Q22.9Congenital malformation of tricuspid valve, unspecified
• Q23.0Congenital stenosis of aortic valve
• Q23.1Congenital insufficiency of aortic valve
• Q23.2Congenital mitral stenosis
• Q23.3Congenital mitral insufficiency
• Q23.4Hypoplastic left heart syndrome
• Q23.81Bicuspid aortic valve
• Q23.82Congenital mitral valve cleft leaflet
• Q23.88Other congenital malformations of aortic and mitral valves
• Q23.9Congenital malformation of aortic and mitral valves, unspecified
• Q24.0Dextrocardia
• Q24.1Levocardia
• Q24.2Cor triatriatum
• Q24.3Pulmonary infundibular stenosis
• Q24.4Congenital subaortic stenosis
• Q24.5Malformation of coronary vessels
• Q24.6Congenital heart block
• Q24.8Other specified congenital malformations of heart
• Q24.9Congenital malformation of heart, unspecified
• Q25.0Patent ductus arteriosus
• Q25.1Coarctation of aorta
• Q25.21Interruption of aortic arch
• Q25.29Other atresia of aorta
• Q25.3Supravalvular aortic stenosis
• Q25.40Congenital malformation of aorta unspecified
• Q25.41Absence and aplasia of aorta
• Q25.42Hypoplasia of aorta
• Q25.43Congenital aneurysm of aorta
• Q25.44Congenital dilation of aorta
• Q25.45Double aortic arch
• Q25.46Tortuous aortic arch
• Q25.47Right aortic arch
• Q25.48Anomalous origin of subclavian artery
• Q25.49Other congenital malformations of aorta
• Q25.5Atresia of pulmonary artery
• Q25.6Stenosis of pulmonary artery
• Q25.71Coarctation of pulmonary artery
• Q25.72Congenital pulmonary arteriovenous malformation
• Q25.79Other congenital malformations of pulmonary artery
• Q25.8Other congenital malformations of other great arteries
• Q25.9Congenital malformation of great arteries, unspecified
• Q26.0Congenital stenosis of vena cava
• Q26.1Persistent left superior vena cava
• Q26.2Total anomalous pulmonary venous connection
• Q26.3Partial anomalous pulmonary venous connection
• Q26.4Anomalous pulmonary venous connection, unspecified
• Q26.5Anomalous portal venous connection
• Q26.6Portal vein-hepatic artery fistula
• Q26.8Other congenital malformations of great veins
• Q26.9Congenital malformation of great vein, unspecified
• Q27.0Congenital absence and hypoplasia of umbilical artery
• Q27.1Congenital renal artery stenosis
• Q27.2Other congenital malformations of renal artery
• Q27.30Arteriovenous malformation, site unspecified
• Q27.31Arteriovenous malformation of vessel of upper limb
• Q27.32Arteriovenous malformation of vessel of lower limb
• Q27.33Arteriovenous malformation of digestive system vessel
• Q27.34Arteriovenous malformation of renal vessel
• Q27.39Arteriovenous malformation, other site
• Q27.4Congenital phlebectasia
• Q27.8Other specified congenital malformations of peripheral vascular system
• Q27.9Congenital malformation of peripheral vascular system, unspecified
• Q28.0Arteriovenous malformation of precerebral vessels
• Q28.1Other malformations of precerebral vessels
• Q28.2Arteriovenous malformation of cerebral vessels
• Q28.3Other malformations of cerebral vessels
• Q28.8Other specified congenital malformations of circulatory system
• Q28.9Congenital malformation of circulatory system, unspecified
• Q30.0Choanal atresia
• Q30.1Agenesis and underdevelopment of nose
• Q30.2Fissured, notched and cleft nose
• Q30.3Congenital perforated nasal septum
• Q30.8Other congenital malformations of nose
• Q30.9Congenital malformation of nose, unspecified
• Q31.0Web of larynx
• Q31.1Congenital subglottic stenosis
• Q31.2Laryngeal hypoplasia
• Q31.3Laryngocele
• Q31.5Congenital laryngomalacia
• Q31.8Other congenital malformations of larynx
• Q31.9Congenital malformation of larynx, unspecified
• Q32.0Congenital tracheomalacia
• Q32.1Other congenital malformations of trachea
• Q32.2Congenital bronchomalacia
• Q32.3Congenital stenosis of bronchus
• Q32.4Other congenital malformations of bronchus
• Q33.0Congenital cystic lung
• Q33.1Accessory lobe of lung
• Q33.2Sequestration of lung
• Q33.3Agenesis of lung
• Q33.4Congenital bronchiectasis
• Q33.5Ectopic tissue in lung
• Q33.6Congenital hypoplasia and dysplasia of lung
• Q33.8Other congenital malformations of lung
• Q33.9Congenital malformation of lung, unspecified
• Q34.0Anomaly of pleura
• Q34.1Congenital cyst of mediastinum
• Q34.8Other specified congenital malformations of respiratory system
• Q34.9Congenital malformation of respiratory system, unspecified
• Q35.1Cleft hard palate
• Q35.3Cleft soft palate
• Q35.5Cleft hard palate with cleft soft palate
• Q35.7Cleft uvula
• Q35.9Cleft palate, unspecified
• Q36.0Cleft lip, bilateral
• Q36.1Cleft lip, median
• Q36.9Cleft lip, unilateral
• Q37.0Cleft hard palate with bilateral cleft lip
• Q37.1Cleft hard palate with unilateral cleft lip
• Q37.2Cleft soft palate with bilateral cleft lip
• Q37.3Cleft soft palate with unilateral cleft lip
• Q37.4Cleft hard and soft palate with bilateral cleft lip
• Q37.5Cleft hard and soft palate with unilateral cleft lip
• Q37.8Unspecified cleft palate with bilateral cleft lip
• Q37.9Unspecified cleft palate with unilateral cleft lip
• Q38.0Congenital malformations of lips, not elsewhere classified
• Q38.1Ankyloglossia
• Q38.2Macroglossia
• Q38.3Other congenital malformations of tongue
• Q38.4Congenital malformations of salivary glands and ducts
• Q38.5Congenital malformations of palate, not elsewhere classified
• Q38.6Other congenital malformations of mouth
• Q38.7Congenital pharyngeal pouch
• Q38.8Other congenital malformations of pharynx
• Q39.0Atresia of esophagus without fistula
• Q39.1Atresia of esophagus with tracheo-esophageal fistula
• Q39.2Congenital tracheo-esophageal fistula without atresia
• Q39.3Congenital stenosis and stricture of esophagus
• Q39.4Esophageal web
• Q39.5Congenital dilatation of esophagus
• Q39.6Congenital diverticulum of esophagus
• Q39.8Other congenital malformations of esophagus
• Q39.9Congenital malformation of esophagus, unspecified
• Q40.0Congenital hypertrophic pyloric stenosis
• Q40.1Congenital hiatus hernia
• Q40.2Other specified congenital malformations of stomach
• Q40.3Congenital malformation of stomach, unspecified
• Q40.8Other specified congenital malformations of upper alimentary tract
• Q40.9Congenital malformation of upper alimentary tract, unspecified
• Q41.0Congenital absence, atresia and stenosis of duodenum
• Q41.1Congenital absence, atresia and stenosis of jejunum
• Q41.2Congenital absence, atresia and stenosis of ileum
• Q41.8Congenital absence, atresia and stenosis of other specified parts of small intestine
• Q41.9Congenital absence, atresia and stenosis of small intestine, part unspecified
• Q42.0Congenital absence, atresia and stenosis of rectum with fistula
• Q42.1Congenital absence, atresia and stenosis of rectum without fistula
• Q42.2Congenital absence, atresia and stenosis of anus with fistula
• Q42.3Congenital absence, atresia and stenosis of anus without fistula
• Q42.8Congenital absence, atresia and stenosis of other parts of large intestine
• Q42.9Congenital absence, atresia and stenosis of large intestine, part unspecified
• Q43.0Meckel's diverticulum (displaced) (hypertrophic)
• Q43.1Hirschsprung's disease
• Q43.2Other congenital functional disorders of colon
• Q43.3Congenital malformations of intestinal fixation
• Q43.4Duplication of intestine
• Q43.5Ectopic anus
• Q43.6Congenital fistula of rectum and anus
• Q43.7Persistent cloaca
• Q43.8Other specified congenital malformations of intestine
• Q43.9Congenital malformation of intestine, unspecified
• Q44.0Agenesis, aplasia and hypoplasia of gallbladder
• Q44.1Other congenital malformations of gallbladder
• Q44.2Atresia of bile ducts
• Q44.3Congenital stenosis and stricture of bile ducts
• Q44.4Choledochal cyst
• Q44.5Other congenital malformations of bile ducts
• Q44.6Cystic disease of liver
• Q44.70Other congenital malformation of liver, unspecified
• Q44.71Alagille syndrome
• Q44.79Other congenital malformations of liver
• Q45.0Agenesis, aplasia and hypoplasia of pancreas
• Q45.1Annular pancreas
• Q45.2Congenital pancreatic cyst
• Q45.3Other congenital malformations of pancreas and pancreatic duct
• Q45.8Other specified congenital malformations of digestive system
• Q45.9Congenital malformation of digestive system, unspecified
• Q50.01Congenital absence of ovary, unilateral
• Q50.02Congenital absence of ovary, bilateral
• Q50.1Developmental ovarian cyst
• Q50.2Congenital torsion of ovary
• Q50.31Accessory ovary
• Q50.32Ovarian streak
• Q50.39Other congenital malformation of ovary
• Q50.4Embryonic cyst of fallopian tube
• Q50.5Embryonic cyst of broad ligament
• Q50.6Other congenital malformations of fallopian tube and broad ligament
• Q51.0Agenesis and aplasia of uterus
• Q51.10Doubling of uterus with doubling of cervix and vagina without obstruction
• Q51.11Doubling of uterus with doubling of cervix and vagina with obstruction
• Q51.21Complete doubling of uterus
• Q51.22Partial doubling of uterus
• Q51.28Other and unspecified doubling of uterus
• Q51.3Bicornate uterus
• Q51.4Unicornate uterus
• Q51.5Agenesis and aplasia of cervix
• Q51.6Embryonic cyst of cervix
• Q51.7Congenital fistulae between uterus and digestive and urinary tracts
• Q51.810Arcuate uterus
• Q51.811Hypoplasia of uterus
• Q51.818Other congenital malformations of uterus
• Q51.820Cervical duplication
• Q51.821Hypoplasia of cervix
• Q51.828Other congenital malformations of cervix
• Q51.9Congenital malformation of uterus and cervix, unspecified
• Q52.0Congenital absence of vagina
• Q52.10Doubling of vagina, unspecified
• Q52.11Transverse vaginal septum
• Q52.120Longitudinal vaginal septum, nonobstructing
• Q52.121Longitudinal vaginal septum, obstructing, right side
• Q52.122Longitudinal vaginal septum, obstructing, left side
• Q52.123Longitudinal vaginal septum, microperforate, right side
• Q52.124Longitudinal vaginal septum, microperforate, left side
• Q52.129Other and unspecified longitudinal vaginal septum
• Q52.2Congenital rectovaginal fistula
• Q52.3Imperforate hymen
• Q52.4Other congenital malformations of vagina
• Q52.5Fusion of labia
• Q52.6Congenital malformation of clitoris
• Q52.70Unspecified congenital malformations of vulva
• Q52.71Congenital absence of vulva
• Q52.79Other congenital malformations of vulva
• Q52.8Other specified congenital malformations of female genitalia
• Q52.9Congenital malformation of female genitalia, unspecified
• Q53.00Ectopic testis, unspecified
• Q53.01Ectopic testis, unilateral
• Q53.02Ectopic testes, bilateral
• Q53.10Unspecified undescended testicle, unilateral
• Q53.111Unilateral intraabdominal testis
• Q53.112Unilateral inguinal testis
• Q53.12Ectopic perineal testis, unilateral
• Q53.13Unilateral high scrotal testis
• Q53.20Undescended testicle, unspecified, bilateral
• Q53.211Bilateral intraabdominal testes
• Q53.212Bilateral inguinal testes
• Q53.22Ectopic perineal testis, bilateral
• Q53.23Bilateral high scrotal testes
• Q53.9Undescended testicle, unspecified
• Q54.0Hypospadias, balanic
• Q54.1Hypospadias, penile
• Q54.2Hypospadias, penoscrotal
• Q54.3Hypospadias, perineal
• Q54.4Congenital chordee
• Q54.8Other hypospadias
• Q54.9Hypospadias, unspecified
• Q55.0Absence and aplasia of testis
• Q55.1Hypoplasia of testis and scrotum
• Q55.20Unspecified congenital malformations of testis and scrotum
• Q55.21Polyorchism
• Q55.22Retractile testis
• Q55.23Scrotal transposition
• Q55.29Other congenital malformations of testis and scrotum
• Q55.3Atresia of vas deferens
• Q55.4Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
• Q55.5Congenital absence and aplasia of penis
• Q55.61Curvature of penis (lateral)
• Q55.62Hypoplasia of penis
• Q55.63Congenital torsion of penis
• Q55.64Hidden penis
• Q55.69Other congenital malformation of penis
• Q55.7Congenital vasocutaneous fistula
• Q55.8Other specified congenital malformations of male genital organs
• Q55.9Congenital malformation of male genital organ, unspecified
• Q56.0Hermaphroditism, not elsewhere classified
• Q56.1Male pseudohermaphroditism, not elsewhere classified
• Q56.2Female pseudohermaphroditism, not elsewhere classified
• Q56.3Pseudohermaphroditism, unspecified
• Q56.4Indeterminate sex, unspecified
• Q60.0Renal agenesis, unilateral
• Q60.1Renal agenesis, bilateral
• Q60.2Renal agenesis, unspecified
• Q60.3Renal hypoplasia, unilateral
• Q60.4Renal hypoplasia, bilateral
• Q60.5Renal hypoplasia, unspecified
• Q60.6Potter's syndrome
• Q61.00Congenital renal cyst, unspecified
• Q61.01Congenital single renal cyst
• Q61.02Congenital multiple renal cysts
• Q61.11Cystic dilatation of collecting ducts
• Q61.19Other polycystic kidney, infantile type
• Q61.2Polycystic kidney, adult type
• Q61.3Polycystic kidney, unspecified
• Q61.4Renal dysplasia
• Q61.5Medullary cystic kidney
• Q61.8Other cystic kidney diseases
• Q61.9Cystic kidney disease, unspecified
• Q62.0Congenital hydronephrosis
• Q62.10Congenital occlusion of ureter, unspecified
• Q62.11Congenital occlusion of ureteropelvic junction
• Q62.12Congenital occlusion of ureterovesical orifice
• Q62.2Congenital megaureter
• Q62.31Congenital ureterocele, orthotopic
• Q62.32Cecoureterocele
• Q62.39Other obstructive defects of renal pelvis and ureter
• Q62.4Agenesis of ureter
• Q62.5Duplication of ureter
• Q62.60Malposition of ureter, unspecified
• Q62.61Deviation of ureter
• Q62.62Displacement of ureter
• Q62.63Anomalous implantation of ureter
• Q62.69Other malposition of ureter
• Q62.7Congenital vesico-uretero-renal reflux
• Q62.8Other congenital malformations of ureter
• Q63.0Accessory kidney
• Q63.1Lobulated, fused and horseshoe kidney
• Q63.2Ectopic kidney
• Q63.3Hyperplastic and giant kidney
• Q63.8Other specified congenital malformations of kidney
• Q63.9Congenital malformation of kidney, unspecified
• Q64.0Epispadias
• Q64.10Exstrophy of urinary bladder, unspecified
• Q64.11Supravesical fissure of urinary bladder
• Q64.12Cloacal exstrophy of urinary bladder
• Q64.19Other exstrophy of urinary bladder
• Q64.2Congenital posterior urethral valves
• Q64.31Congenital bladder neck obstruction
• Q64.32Congenital stricture of urethra
• Q64.33Congenital stricture of urinary meatus
• Q64.39Other atresia and stenosis of urethra and bladder neck
• Q64.4Malformation of urachus
• Q64.5Congenital absence of bladder and urethra
• Q64.6Congenital diverticulum of bladder
• Q64.70Unspecified congenital malformation of bladder and urethra
• Q64.71Congenital prolapse of urethra
• Q64.72Congenital prolapse of urinary meatus
• Q64.73Congenital urethrorectal fistula
• Q64.74Double urethra
• Q64.75Double urinary meatus
• Q64.79Other congenital malformations of bladder and urethra
• Q64.8Other specified congenital malformations of urinary system
• Q64.9Congenital malformation of urinary system, unspecified
• Q65.00Congenital dislocation of unspecified hip, unilateral
• Q65.01Congenital dislocation of right hip, unilateral
• Q65.02Congenital dislocation of left hip, unilateral
• Q65.1Congenital dislocation of hip, bilateral
• Q65.2Congenital dislocation of hip, unspecified
• Q65.30Congenital partial dislocation of unspecified hip, unilateral
• Q65.31Congenital partial dislocation of right hip, unilateral
• Q65.32Congenital partial dislocation of left hip, unilateral
• Q65.4Congenital partial dislocation of hip, bilateral
• Q65.5Congenital partial dislocation of hip, unspecified
• Q65.6Congenital unstable hip
• Q65.81Congenital coxa valga
• Q65.82Congenital coxa vara
• Q65.89Other specified congenital deformities of hip
• Q65.9Congenital deformity of hip, unspecified
• Q66.00Congenital talipes equinovarus, unspecified foot
• Q66.01Congenital talipes equinovarus, right foot
• Q66.02Congenital talipes equinovarus, left foot
• Q66.10Congenital talipes calcaneovarus, unspecified foot
• Q66.11Congenital talipes calcaneovarus, right foot
• Q66.12Congenital talipes calcaneovarus, left foot
• Q66.211Congenital metatarsus primus varus, right foot
• Q66.212Congenital metatarsus primus varus, left foot
• Q66.219Congenital metatarsus primus varus, unspecified foot
• Q66.221Congenital metatarsus adductus, right foot
• Q66.222Congenital metatarsus adductus, left foot
• Q66.229Congenital metatarsus adductus, unspecified foot
• Q66.30Other congenital varus deformities of feet, unspecified foot
• Q66.31Other congenital varus deformities of feet, right foot
• Q66.32Other congenital varus deformities of feet, left foot
• Q66.40Congenital talipes calcaneovalgus, unspecified foot
• Q66.41Congenital talipes calcaneovalgus, right foot
• Q66.42Congenital talipes calcaneovalgus, left foot
• Q66.50Congenital pes planus, unspecified foot
• Q66.51Congenital pes planus, right foot
• Q66.52Congenital pes planus, left foot
• Q66.6Other congenital valgus deformities of feet
• Q66.70Congenital pes cavus, unspecified foot
• Q66.71Congenital pes cavus, right foot
• Q66.72Congenital pes cavus, left foot
• Q66.80Congenital vertical talus deformity, unspecified foot
• Q66.81Congenital vertical talus deformity, right foot
• Q66.82Congenital vertical talus deformity, left foot
• Q66.89Other specified congenital deformities of feet
• Q66.90Congenital deformity of feet, unspecified, unspecified foot
• Q66.91Congenital deformity of feet, unspecified, right foot
• Q66.92Congenital deformity of feet, unspecified, left foot
• Q67.0Congenital facial asymmetry
• Q67.1Congenital compression facies
• Q67.2Dolichocephaly
• Q67.3Plagiocephaly
• Q67.4Other congenital deformities of skull, face and jaw
• Q67.5Congenital deformity of spine
• Q67.6Pectus excavatum
• Q67.7Pectus carinatum
• Q67.8Other congenital deformities of chest
• Q68.0Congenital deformity of sternocleidomastoid muscle
• Q68.1Congenital deformity of finger(s) and hand
• Q68.2Congenital deformity of knee
• Q68.3Congenital bowing of femur
• Q68.4Congenital bowing of tibia and fibula
• Q68.5Congenital bowing of long bones of leg, unspecified
• Q68.6Discoid meniscus
• Q68.8Other specified congenital musculoskeletal deformities
• Q69.0Accessory finger(s)
• Q69.1Accessory thumb(s)
• Q69.2Accessory toe(s)
• Q69.9Polydactyly, unspecified
• Q70.00Fused fingers, unspecified hand
• Q70.01Fused fingers, right hand
• Q70.02Fused fingers, left hand
• Q70.03Fused fingers, bilateral
• Q70.10Webbed fingers, unspecified hand
• Q70.11Webbed fingers, right hand
• Q70.12Webbed fingers, left hand
• Q70.13Webbed fingers, bilateral
• Q70.20Fused toes, unspecified foot
• Q70.21Fused toes, right foot
• Q70.22Fused toes, left foot
• Q70.23Fused toes, bilateral
• Q70.30Webbed toes, unspecified foot
• Q70.31Webbed toes, right foot
• Q70.32Webbed toes, left foot
• Q70.33Webbed toes, bilateral
• Q70.4Polysyndactyly, unspecified
• Q70.9Syndactyly, unspecified
• Q71.00Congenital complete absence of unspecified upper limb
• Q71.01Congenital complete absence of right upper limb
• Q71.02Congenital complete absence of left upper limb
• Q71.03Congenital complete absence of upper limb, bilateral
• Q71.10Congenital absence of unspecified upper arm and forearm with hand present
• Q71.11Congenital absence of right upper arm and forearm with hand present
• Q71.12Congenital absence of left upper arm and forearm with hand present
• Q71.13Congenital absence of upper arm and forearm with hand present, bilateral
• Q71.20Congenital absence of both forearm and hand, unspecified upper limb
• Q71.21Congenital absence of both forearm and hand, right upper limb
• Q71.22Congenital absence of both forearm and hand, left upper limb
• Q71.23Congenital absence of both forearm and hand, bilateral
• Q71.30Congenital absence of unspecified hand and finger
• Q71.31Congenital absence of right hand and finger
• Q71.32Congenital absence of left hand and finger
• Q71.33Congenital absence of hand and finger, bilateral
• Q71.40Longitudinal reduction defect of unspecified radius
• Q71.41Longitudinal reduction defect of right radius
• Q71.42Longitudinal reduction defect of left radius
• Q71.43Longitudinal reduction defect of radius, bilateral
• Q71.50Longitudinal reduction defect of unspecified ulna
• Q71.51Longitudinal reduction defect of right ulna
• Q71.52Longitudinal reduction defect of left ulna
• Q71.53Longitudinal reduction defect of ulna, bilateral
• Q71.60Lobster-claw hand, unspecified hand
• Q71.61Lobster-claw right hand
• Q71.62Lobster-claw left hand
• Q71.63Lobster-claw hand, bilateral
• Q71.811Congenital shortening of right upper limb
• Q71.812Congenital shortening of left upper limb
• Q71.813Congenital shortening of upper limb, bilateral
• Q71.819Congenital shortening of unspecified upper limb
• Q71.891Other reduction defects of right upper limb
• Q71.892Other reduction defects of left upper limb
• Q71.893Other reduction defects of upper limb, bilateral
• Q71.899Other reduction defects of unspecified upper limb
• Q71.90Unspecified reduction defect of unspecified upper limb
• Q71.91Unspecified reduction defect of right upper limb
• Q71.92Unspecified reduction defect of left upper limb
• Q71.93Unspecified reduction defect of upper limb, bilateral
• Q72.00Congenital complete absence of unspecified lower limb
• Q72.01Congenital complete absence of right lower limb
• Q72.02Congenital complete absence of left lower limb
• Q72.03Congenital complete absence of lower limb, bilateral
• Q72.10Congenital absence of unspecified thigh and lower leg with foot present
• Q72.11Congenital absence of right thigh and lower leg with foot present
• Q72.12Congenital absence of left thigh and lower leg with foot present
• Q72.13Congenital absence of thigh and lower leg with foot present, bilateral
• Q72.20Congenital absence of both lower leg and foot, unspecified lower limb
• Q72.21Congenital absence of both lower leg and foot, right lower limb
• Q72.22Congenital absence of both lower leg and foot, left lower limb
• Q72.23Congenital absence of both lower leg and foot, bilateral
• Q72.30Congenital absence of unspecified foot and toe(s)
• Q72.31Congenital absence of right foot and toe(s)
• Q72.32Congenital absence of left foot and toe(s)
• Q72.33Congenital absence of foot and toe(s), bilateral
• Q72.40Longitudinal reduction defect of unspecified femur
• Q72.41Longitudinal reduction defect of right femur
• Q72.42Longitudinal reduction defect of left femur
• Q72.43Longitudinal reduction defect of femur, bilateral
• Q72.50Longitudinal reduction defect of unspecified tibia
• Q72.51Longitudinal reduction defect of right tibia
• Q72.52Longitudinal reduction defect of left tibia
• Q72.53Longitudinal reduction defect of tibia, bilateral
• Q72.60Longitudinal reduction defect of unspecified fibula
• Q72.61Longitudinal reduction defect of right fibula
• Q72.62Longitudinal reduction defect of left fibula
• Q72.63Longitudinal reduction defect of fibula, bilateral
• Q72.70Split foot, unspecified lower limb
• Q72.71Split foot, right lower limb
• Q72.72Split foot, left lower limb
• Q72.73Split foot, bilateral
• Q72.811Congenital shortening of right lower limb
• Q72.812Congenital shortening of left lower limb
• Q72.813Congenital shortening of lower limb, bilateral
• Q72.819Congenital shortening of unspecified lower limb
• Q72.891Other reduction defects of right lower limb
• Q72.892Other reduction defects of left lower limb
• Q72.893Other reduction defects of lower limb, bilateral
• Q72.899Other reduction defects of unspecified lower limb
• Q72.90Unspecified reduction defect of unspecified lower limb
• Q72.91Unspecified reduction defect of right lower limb
• Q72.92Unspecified reduction defect of left lower limb
• Q72.93Unspecified reduction defect of lower limb, bilateral
• Q73.0Congenital absence of unspecified limb(s)
• Q73.1Phocomelia, unspecified limb(s)
• Q73.8Other reduction defects of unspecified limb(s)
• Q74.0Other congenital malformations of upper limb(s), including shoulder girdle
• Q74.1Congenital malformation of knee
• Q74.2Other congenital malformations of lower limb(s), including pelvic girdle
• Q74.3Arthrogryposis multiplex congenita
• Q74.8Other specified congenital malformations of limb(s)
• Q74.9Unspecified congenital malformation of limb(s)
• Q75.001Craniosynostosis, unspecified type, unilateral
• Q75.002Craniosynostosis, unspecified type, bilateral
• Q75.009Craniosynostosis, unspecified
• Q75.01Sagittal craniosynostosis
• Q75.021Coronal craniosynostosis, unilateral
• Q75.022Coronal craniosynostosis, bilateral
• Q75.029Coronal craniosynostosis, unspecified
• Q75.03Metopic craniosynostosis
• Q75.041Lambdoid craniosynostosis, unilateral
• Q75.042Lambdoid craniosynostosis, bilateral
• Q75.049Lambdoid craniosynostosis, unspecified
• Q75.051Cloverleaf skull
• Q75.052Pansynostosis
• Q75.058Other multi-suture craniosynostosis
• Q75.08Other single-suture craniosynostosis
• Q75.1Craniofacial dysostosis
• Q75.2Hypertelorism
• Q75.3Macrocephaly
• Q75.4Mandibulofacial dysostosis
• Q75.5Oculomandibular dysostosis
• Q75.8Other specified congenital malformations of skull and face bones
• Q75.9Congenital malformation of skull and face bones, unspecified
• Q76.0Spina bifida occulta
• Q76.1Klippel-Feil syndrome
• Q76.2Congenital spondylolisthesis
• Q76.3Congenital scoliosis due to congenital bony malformation
• Q76.411Congenital kyphosis, occipito-atlanto-axial region
• Q76.412Congenital kyphosis, cervical region
• Q76.413Congenital kyphosis, cervicothoracic region
• Q76.414Congenital kyphosis, thoracic region
• Q76.415Congenital kyphosis, thoracolumbar region
• Q76.419Congenital kyphosis, unspecified region
• Q76.425Congenital lordosis, thoracolumbar region
• Q76.426Congenital lordosis, lumbar region
• Q76.427Congenital lordosis, lumbosacral region
• Q76.428Congenital lordosis, sacral and sacrococcygeal region
• Q76.429Congenital lordosis, unspecified region
• Q76.49Other congenital malformations of spine, not associated with scoliosis
• Q76.5Cervical rib
• Q76.6Other congenital malformations of ribs
• Q76.7Congenital malformation of sternum
• Q76.8Other congenital malformations of bony thorax
• Q76.9Congenital malformation of bony thorax, unspecified
• Q77.0Achondrogenesis
• Q77.1Thanatophoric short stature
• Q77.2Short rib syndrome
• Q77.3Chondrodysplasia punctata
• Q77.4Achondroplasia
• Q77.5Diastrophic dysplasia
• Q77.6Chondroectodermal dysplasia
• Q77.7Spondyloepiphyseal dysplasia
• Q77.8Other osteochondrodysplasia with defects of growth of tubular bones and spine
• Q77.9Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
• Q78.0Osteogenesis imperfecta
• Q78.1Polyostotic fibrous dysplasia
• Q78.2Osteopetrosis
• Q78.3Progressive diaphyseal dysplasia
• Q78.4Enchondromatosis
• Q78.5Metaphyseal dysplasia
• Q78.6Multiple congenital exostoses
• Q78.8Other specified osteochondrodysplasias
• Q78.9Osteochondrodysplasia, unspecified
• Q79.0Congenital diaphragmatic hernia
• Q79.1Other congenital malformations of diaphragm
• Q79.2Exomphalos
• Q79.3Gastroschisis
• Q79.4Prune belly syndrome
• Q79.51Congenital hernia of bladder
• Q79.59Other congenital malformations of abdominal wall
• Q79.60Ehlers-Danlos syndrome, unspecified
• Q79.61Classical Ehlers-Danlos syndrome
• Q79.62Hypermobile Ehlers-Danlos syndrome
• Q79.63Vascular Ehlers-Danlos syndrome
• Q79.69Other Ehlers-Danlos syndromes
• Q79.8Other congenital malformations of musculoskeletal system
• Q79.9Congenital malformation of musculoskeletal system, unspecified
• Q80.0Ichthyosis vulgaris
• Q80.1X-linked ichthyosis
• Q80.2Lamellar ichthyosis
• Q80.3Congenital bullous ichthyosiform erythroderma
• Q80.4Harlequin fetus
• Q80.8Other congenital ichthyosis
• Q80.9Congenital ichthyosis, unspecified
• Q81.0Epidermolysis bullosa simplex
• Q81.1Epidermolysis bullosa letalis
• Q81.2Epidermolysis bullosa dystrophica
• Q81.8Other epidermolysis bullosa
• Q81.9Epidermolysis bullosa, unspecified
• Q82.0Hereditary lymphedema
• Q82.1Xeroderma pigmentosum
• Q82.2Congenital cutaneous mastocytosis
• Q82.3Incontinentia pigmenti
• Q82.4Ectodermal dysplasia (anhidrotic)
• Q82.5Congenital non-neoplastic nevus
• Q82.6Congenital sacral dimple
• Q82.8Other specified congenital malformations of skin
• Q82.9Congenital malformation of skin, unspecified
• Q83.0Congenital absence of breast with absent nipple
• Q83.1Accessory breast
• Q83.2Absent nipple
• Q83.3Accessory nipple
• Q83.8Other congenital malformations of breast
• Q83.9Congenital malformation of breast, unspecified
• Q84.0Congenital alopecia
• Q84.1Congenital morphological disturbances of hair, not elsewhere classified
• Q84.2Other congenital malformations of hair
• Q84.3Anonychia
• Q84.4Congenital leukonychia
• Q84.5Enlarged and hypertrophic nails
• Q84.6Other congenital malformations of nails
• Q84.8Other specified congenital malformations of integument
• Q84.9Congenital malformation of integument, unspecified
• Q85.00Neurofibromatosis, unspecified
• Q85.01Neurofibromatosis, type 1
• Q85.02Neurofibromatosis, type 2
• Q85.03Schwannomatosis
• Q85.09Other neurofibromatosis
• Q85.1Tuberous sclerosis
• Q85.81PTEN hamartoma tumor syndrome
• Q85.82Other Cowden syndrome
• Q85.83Von Hippel-Lindau syndrome
• Q85.89Other phakomatoses, not elsewhere classified
• Q85.9Phakomatosis, unspecified
• Q86.0Fetal alcohol syndrome (dysmorphic)
• Q86.1Fetal hydantoin syndrome
• Q86.2Dysmorphism due to warfarin
• Q86.8Other congenital malformation syndromes due to known exogenous causes
• Q87.0Congenital malformation syndromes predominantly affecting facial appearance
• Q87.11Prader-Willi syndrome
• Q87.19Other congenital malformation syndromes predominantly associated with short stature
• Q87.2Congenital malformation syndromes predominantly involving limbs
• Q87.3Congenital malformation syndromes involving early overgrowth
• Q87.40Marfan syndrome, unspecified
• Q87.410Marfan syndrome with aortic dilation
• Q87.418Marfan syndrome with other cardiovascular manifestations
• Q87.42Marfan syndrome with ocular manifestations
• Q87.43Marfan syndrome with skeletal manifestation
• Q87.5Other congenital malformation syndromes with other skeletal changes
• Q87.81Alport syndrome
• Q87.82Arterial tortuosity syndrome
• Q87.83Bardet-Biedl syndrome
• Q87.84Laurence-Moon syndrome
• Q87.85MED13L syndrome
• Q87.86Kleefstra syndrome
• Q87.87Hao-Fountain Syndrome
• Q87.88CTNNB1 syndrome
• Q87.89Other specified congenital malformation syndromes, not elsewhere classified
• Q87.ALoeys-Dietz syndrome
• Q89.01Asplenia (congenital)
• Q89.09Congenital malformations of spleen
• Q89.1Congenital malformations of adrenal gland
• Q89.2Congenital malformations of other endocrine glands
• Q89.3Situs inversus
• Q89.4Conjoined twins
• Q89.7Multiple congenital malformations, not elsewhere classified
• Q89.81Kabuki syndrome
• Q89.89Other specified congenital malformations
• Q89.9Congenital malformation, unspecified
• Q90.0Trisomy 21, nonmosaicism (meiotic nondisjunction)
• Q90.1Trisomy 21, mosaicism (mitotic nondisjunction)
• Q90.2Trisomy 21, translocation
• Q90.9Down syndrome, unspecified
• Q91.0Trisomy 18, nonmosaicism (meiotic nondisjunction)
• Q91.1Trisomy 18, mosaicism (mitotic nondisjunction)
• Q91.2Trisomy 18, translocation
• Q91.3Trisomy 18, unspecified
• Q91.4Trisomy 13, nonmosaicism (meiotic nondisjunction)
• Q91.5Trisomy 13, mosaicism (mitotic nondisjunction)
• Q91.6Trisomy 13, translocation
• Q91.7Trisomy 13, unspecified
• Q92.0Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
• Q92.1Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
• Q92.2Partial trisomy
• Q92.5Duplications with other complex rearrangements
• Q92.61Marker chromosomes in normal individual
• Q92.62Marker chromosomes in abnormal individual
• Q92.7Triploidy and polyploidy
• Q92.8Other specified trisomies and partial trisomies of autosomes
• Q92.9Trisomy and partial trisomy of autosomes, unspecified
• Q93.0Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
• Q93.1Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
• Q93.2Chromosome replaced with ring, dicentric or isochromosome
• Q93.3Deletion of short arm of chromosome 4
• Q93.4Deletion of short arm of chromosome 5
• Q93.51Angelman syndrome
• Q93.52Phelan-McDermid syndrome
• Q93.59Other deletions of part of a chromosome
• Q93.7Deletions with other complex rearrangements
• Q93.81Velo-cardio-facial syndrome
• Q93.82Williams syndrome
• Q93.88Other microdeletions
• Q93.89Other deletions from the autosomes
• Q93.9Deletion from autosomes, unspecified
• Q95.0Balanced translocation and insertion in normal individual
• Q95.1Chromosome inversion in normal individual
• Q95.2Balanced autosomal rearrangement in abnormal individual
• Q95.3Balanced sex/autosomal rearrangement in abnormal individual
• Q95.5Individual with autosomal fragile site
• Q95.8Other balanced rearrangements and structural markers
• Q95.9Balanced rearrangement and structural marker, unspecified
• Q96.0Karyotype 45, X
• Q96.1Karyotype 46, X iso (Xq)
• Q96.2Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
• Q96.3Mosaicism, 45, X/46, XX or XY
• Q96.4Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
• Q96.8Other variants of Turner's syndrome
• Q96.9Turner's syndrome, unspecified
• Q97.0Karyotype 47, XXX
• Q97.1Female with more than three X chromosomes
• Q97.2Mosaicism, lines with various numbers of X chromosomes
• Q97.3Female with 46, XY karyotype
• Q97.8Other specified sex chromosome abnormalities, female phenotype
• Q97.9Sex chromosome abnormality, female phenotype, unspecified
• Q98.0Klinefelter syndrome karyotype 47, XXY
• Q98.1Klinefelter syndrome, male with more than two X chromosomes
• Q98.3Other male with 46, XX karyotype
• Q98.4Klinefelter syndrome, unspecified
• Q98.5Karyotype 47, XYY
• Q98.6Male with structurally abnormal sex chromosome
• Q98.7Male with sex chromosome mosaicism
• Q98.8Other specified sex chromosome abnormalities, male phenotype
• Q98.9Sex chromosome abnormality, male phenotype, unspecified
• Q99.0Chimera 46, XX/46, XY
• Q99.146, XX true hermaphrodite
• Q99.2Fragile X chromosome
• Q99.811Usher syndrome, type 1
• Q99.812Usher syndrome, type 2
• Q99.813Usher syndrome, type 3
• Q99.818Other Usher syndrome
• Q99.819Usher syndrome, unspecified
• Q99.89Other specified chromosome abnormalities
• Q99.9Chromosomal abnormality, unspecified
• QA0.0101SCN2A-related neurodevelopmental disorder
• QA0.0102CACNA1A-related neurodevelopmental disorder
• QA0.0109Neurodevelopmental disorder related to pathogenic variant in other ion channel gene
• QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
• QA0.012Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
• QA0.0131SLC6A1-related disorder
• QA0.0139Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene
• QA0.0141Syntaxin-binding protein 1-related disorder
• QA0.0142DLG4-related synaptopathy
• QA0.0149Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene
• QA0.0151FOXG1 syndrome
• QA0.0159Neurodevelopmental disorder, related to other genes associated with transcription and gene expression
• QA0.8Other neurodevelopmental disorders related to pathogenic variants in other specific genes
• QA1.71Lynch syndrome
• QA1.790Familial cancer syndrome with pathogenic BRCA1 mutation
• QA1.791Familial cancer syndrome with pathogenic BRCA2 mutation
• QA1.792Li Fraumeni syndrome
• QA1.798Other inherited neoplasm predisposition syndrome of multiple systems