| Q00 | Anencephaly and similar malformations | ||
| Q00.0 | Anencephaly | ||
| Q00.1 | Craniorachischisis | ||
| Q00.2 | Iniencephaly | ||
| Q01 | Encephalocele | ||
| Q01.0 | Frontal encephalocele | ||
| Q01.1 | Nasofrontal encephalocele | ||
| Q01.2 | Occipital encephalocele | ||
| Q01.8 | Encephalocele of other sites | ||
| Q01.9 | Encephalocele, unspecified | ||
| Q02 | Microcephaly | ||
| Q03 | Congenital hydrocephalus | ||
| Q03.0 | Malformations of aqueduct of Sylvius | ||
| Q03.1 | Atresia of foramina of Magendie and Luschka | ||
| Q03.8 | Other congenital hydrocephalus | ||
| Q03.9 | Congenital hydrocephalus, unspecified | ||
| Q04 | Other congenital malformations of brain | ||
| Q04.0 | Congenital malformations of corpus callosum | ||
| Q04.1 | Arhinencephaly | ||
| Q04.2 | Holoprosencephaly | ||
| Q04.3 | Other reduction deformities of brain | ||
| Q04.4 | Septo-optic dysplasia | ||
| Q04.5 | Megalencephaly | ||
| Q04.6 | Congenital cerebral cysts | ||
| Q04.8 | Other specified congenital malformations of brain | ||
| Q04.9 | Congenital malformation of brain, unspecified | ||
| Q05 | Spina bifida | ||
| Q05.0 | Cervical spina bifida with hydrocephalus | ||
| Q05.1 | Thoracic spina bifida with hydrocephalus | ||
| Q05.2 | Lumbar spina bifida with hydrocephalus | ||
| Q05.3 | Sacral spina bifida with hydrocephalus | ||
| Q05.4 | Unspecified spina bifida with hydrocephalus | ||
| Q05.5 | Cervical spina bifida without hydrocephalus | ||
| Q05.6 | Thoracic spina bifida without hydrocephalus | ||
| Q05.7 | Lumbar spina bifida without hydrocephalus | ||
| Q05.8 | Sacral spina bifida without hydrocephalus | ||
| Q05.9 | Spina bifida, unspecified | ||
| Q06 | Other congenital malformations of spinal cord | ||
| Q06.0 | Amyelia | ||
| Q06.1 | Hypoplasia and dysplasia of spinal cord | ||
| Q06.2 | Diastematomyelia | ||
| Q06.3 | Other congenital cauda equina malformations | ||
| Q06.4 | Hydromyelia | ||
| Q06.8 | Other specified congenital malformations of spinal cord | ||
| Q06.9 | Congenital malformation of spinal cord, unspecified | ||
| Q07 | Other congenital malformations of nervous system | ||
| Q07.0 | Arnold-Chiari syndrome | ||
| Q07.8 | Other specified congenital malformations of nervous system | ||
| Q07.9 | Congenital malformation of nervous system, unspecified | ||
| Q10 | Congenital malformations of eyelid, lacrimal apparatus and orbit | ||
| Q10.0 | Congenital ptosis | ||
| Q10.1 | Congenital ectropion | ||
| Q10.2 | Congenital entropion | ||
| Q10.3 | Other congenital malformations of eyelid | ||
| Q10.4 | Absence and agenesis of lacrimal apparatus | ||
| Q10.5 | Congenital stenosis and stricture of lacrimal duct | ||
| Q10.6 | Other congenital malformations of lacrimal apparatus | ||
| Q10.7 | Congenital malformation of orbit | ||
| Q11 | Anophthalmos, microphthalmos and macrophthalmos | ||
| Q11.0 | Cystic eyeball | ||
| Q11.1 | Other anophthalmos | ||
| Q11.2 | Microphthalmos | ||
| Q11.3 | Macrophthalmos | ||
| Q12 | Congenital lens malformations | ||
| Q12.0 | Congenital cataract | ||
| Q12.1 | Congenital displaced lens | ||
| Q12.2 | Coloboma of lens | ||
| Q12.3 | Congenital aphakia | ||
| Q12.4 | Spherophakia | ||
| Q12.8 | Other congenital lens malformations | ||
| Q12.9 | Congenital lens malformation, unspecified | ||
| Q13 | Congenital malformations of anterior segment of eye | ||
| Q13.0 | Coloboma of iris | ||
| Q13.1 | Absence of iris | ||
| Q13.2 | Other congenital malformations of iris | ||
| Q13.3 | Congenital corneal opacity | ||
| Q13.4 | Other congenital corneal malformations | ||
| Q13.5 | Blue sclera | ||
| Q13.8 | Other congenital malformations of anterior segment of eye | ||
| Q13.9 | Congenital malformation of anterior segment of eye, unspecified | ||
| Q14 | Congenital malformations of posterior segment of eye | ||
| Q14.0 | Congenital malformation of vitreous humour | ||
| Q14.1 | Congenital malformation of retina | ||
| Q14.2 | Congenital malformation of optic disc | ||
| Q14.3 | Congenital malformation of choroid | ||
| Q14.8 | Other congenital malformations of posterior segment of eye | ||
| Q14.9 | Congenital malformation of posterior segment of eye, unspecified | ||
| Q15 | Other congenital malformations of eye | ||
| Q15.0 | Congenital glaucoma | ||
| Q15.8 | Other specified congenital malformations of eye | ||
| Q15.9 | Congenital malformation of eye, unspecified | ||
| Q16 | Congenital malformations of ear causing impairment of hearing | ||
| Q16.0 | Congenital absence of (ear) auricle | ||
| Q16.1 | Congenital absence, atresia and stricture of auditory canal(external) | ||
| Q16.2 | Absence of eustachian tube | ||
| Q16.3 | Congenital malformation of ear ossicles | ||
| Q16.4 | Other congenital malformations of middle ear | ||
| Q16.5 | Congenital malformation of inner ear | ||
| Q16.9 | Congenital malformation of ear causing impairment of hearing,unspecified | ||
| Q17 | Other congenital malformations of ear | ||
| Q17.0 | Accessory auricle | ||
| Q17.1 | Macrotia | ||
| Q17.2 | Microtia | ||
| Q17.3 | Other misshapen ear | ||
| Q17.4 | Misplaced ear | ||
| Q17.5 | Prominent ear | ||
| Q17.8 | Other specified congenital malformations of ear | ||
| Q17.9 | Congenital malformation of ear, unspecified | ||
| Q18 | Other congenital malformations of face and neck | ||
| Q18.0 | Sinus, fistula and cyst of branchial cleft | ||
| Q18.1 | Preauricular sinus and cyst | ||
| Q18.2 | Other branchial cleft malformations | ||
| Q18.3 | Webbing of neck | ||
| Q18.4 | Macrostomia | ||
| Q18.5 | Microstomia | ||
| Q18.6 | Macrocheilia | ||
| Q18.7 | Microcheilia | ||
| Q18.8 | Other specified congenital malformations of face and neck | ||
| Q18.9 | Congenital malformation of face and neck, unspecified | ||
| Q20 | Congenital malformations of cardiac chambers and connections | ||
| Q20.0 | Common arterial trunk | ||
| Q20.1 | Double outlet right ventricle | ||
| Q20.2 | Double outlet left ventricle | ||
| Q20.3 | Discordant ventriculoarterial connection | ||
| Q20.4 | Double inlet ventricle | ||
| Q20.5 | Discordant atrioventricular connection | ||
| Q20.6 | Isomerism of atrial appendages | ||
| Q20.8 | Other congenital malformations of cardiac chambers and connections | ||
| Q20.9 | Congenital malformation of cardiac chambers and connections,unspecified | ||
| Q21 | Congenital malformations of cardiac septa | ||
| Q21.0 | Ventricular septal defect | ||
| Q21.1 | Atrial septal defect | ||
| Q21.2 | Atrioventricular septal defect | ||
| Q21.3 | Tetralogy of Fallot | ||
| Q21.4 | Aortopulmonary septal defect | ||
| Q21.8 | Other congenital malformations of cardiac septa | ||
| Q21.9 | Congenital malformation of cardiac septum, unspecified | ||
| Q22 | Congenital malformations of pulmonary and tricuspid valves | ||
| Q22.0 | Pulmonary valve atresia | ||
| Q22.1 | Congenital pulmonary valve stenosis | ||
| Q22.2 | Congenital pulmonary valve insufficiency | ||
| Q22.3 | Other congenital malformations of pulmonary valve | ||
| Q22.4 | Congenital tricuspid stenosis | ||
| Q22.5 | Ebstein's anomaly | ||
| Q22.6 | Hypoplastic right heart syndrome | ||
| Q22.8 | Other congenital malformations of tricuspid valve | ||
| Q22.9 | Congenital malformation of tricuspid valve, unspecified | ||
| Q23 | Congenital malformations of aortic and mitral valves | ||
| Q23.0 | Congenital stenosis of aortic valve | ||
| Q23.1 | Congenital insufficiency of aortic valve | ||
| Q23.2 | Congenital mitral stenosis | ||
| Q23.3 | Congenital mitral insufficiency | ||
| Q23.4 | Hypoplastic left heart syndrome | ||
| Q23.8 | Other congenital malformations of aortic and mitral valves | ||
| Q23.9 | Congenital malformation of aortic and mitral valves, unspecified | ||
| Q24 | Other congenital malformations of heart | ||
| Q24.0 | Dextrocardia | ||
| Q24.1 | Laevocardia | ||
| Q24.2 | Cor triatriatum | ||
| Q24.3 | Pulmonary infundibular stenosis | ||
| Q24.4 | Congenital subaortic stenosis | ||
| Q24.5 | Malformation of coronary vessels | ||
| Q24.6 | Congenital heart block | ||
| Q24.8 | Other specified congenital malformations of heart | ||
| Q24.9 | Congenital malformation of heart, unspecified | ||
| Q25 | Congenital malformations of great arteries | ||
| Q25.0 | Patent ductus arteriosus | ||
| Q25.1 | Coarctation of aorta | ||
| Q25.2 | Atresia of aorta | ||
| Q25.3 | Stenosis of aorta | ||
| Q25.4 | Other congenital malformations of aorta | ||
| Q25.5 | Atresia of pulmonary artery | ||
| Q25.6 | Stenosis of pulmonary artery | ||
| Q25.7 | Other congenital malformations of pulmonary artery | ||
| Q25.8 | Other congenital malformations of great arteries | ||
| Q25.9 | Congenital malformation of great arteries, unspecified | ||
| Q26 | Congenital malformations of great veins | ||
| Q26.0 | Congenital stenosis of vena cava | ||
| Q26.1 | Persistent left superior vena cava | ||
| Q26.2 | Total anomalous pulmonary venous connection | ||
| Q26.3 | Partial anomalous pulmonary venous connection | ||
| Q26.4 | Anomalous pulmonary venous connection, unspecified | ||
| Q26.5 | Anomalous portal venous connection | ||
| Q26.6 | Portal vein-hepatic artery fistula | ||
| Q26.8 | Other congenital malformations of great veins | ||
| Q26.9 | Congenital malformation of great vein, unspecified | ||
| Q27 | Other congenital malformations of peripheral vascular system | ||
| Q27.0 | Congenital absence and hypoplasia of umbilical artery | ||
| Q27.1 | Congenital renal artery stenosis | ||
| Q27.2 | Other congenital malformations of renal artery | ||
| Q27.3 | Peripheral arteriovenous malformation | ||
| Q27.4 | Congenital phlebectasia | ||
| Q27.8 | Other specified congenital malformations of peripheral vascularsystem | ||
| Q27.9 | Congenital malformation of peripheral vascular system, unspecified | ||
| Q28 | Other congenital malformations of circulatory system | ||
| Q28.0 | Arteriovenous malformation of precerebral vessels | ||
| Q28.1 | Other malformations of precerebral vessels | ||
| Q28.2 | Arteriovenous malformation of cerebral vessels | ||
| Q28.3 | Other malformations of cerebral vessels | ||
| Q28.8 | Other specified congenital malformations of circulatory system | ||
| Q28.9 | Congenital malformation of circulatory system, unspecified | ||
| Q30 | Congenital malformations of nose | ||
| Q30.0 | Choanal atresia | ||
| Q30.1 | Agenesis and underdevelopment of nose | ||
| Q30.2 | Fissured, notched and cleft nose | ||
| Q30.3 | Congenital perforated nasal septum | ||
| Q30.8 | Other congenital malformations of nose | ||
| Q30.9 | Congenital malformation of nose, unspecified | ||
| Q31 | Congenital malformations of larynx | ||
| Q31.0 | Web of larynx | ||
| Q31.1 | Congenital subglottic stenosis | ||
| Q31.2 | Laryngeal hypoplasia | ||
| Q31.3 | Laryngocele | ||
| Q31.4 | Congenital laryngeal stridor | ||
| Q31.8 | Other congenital malformations of larynx | ||
| Q31.9 | Congenital malformation of larynx, unspecified | ||
| Q32 | Congenital malformations of trachea and bronchus | ||
| Q32.0 | Congenital tracheomalacia | ||
| Q32.1 | Other congenital malformations of trachea | ||
| Q32.2 | Congenital bronchomalacia | ||
| Q32.3 | Congenital stenosis of bronchus | ||
| Q32.4 | Other congenital malformations of bronchus | ||
| Q33 | Congenital malformations of lung | ||
| Q33.0 | Congenital cystic lung | ||
| Q33.1 | Accessory lobe of lung | ||
| Q33.2 | Sequestration of lung | ||
| Q33.3 | Agenesis of lung | ||
| Q33.4 | Congenital bronchiectasis | ||
| Q33.5 | Ectopic tissue in lung | ||
| Q33.6 | Hypoplasia and dysplasia of lung | ||
| Q33.8 | Other congenital malformations of lung | ||
| Q33.9 | Congenital malformation of lung, unspecified | ||
| Q34 | Other congenital malformations of respiratory system | ||
| Q34.0 | Anomaly of pleura | ||
| Q34.1 | Congenital cyst of mediastinum | ||
| Q34.8 | Other specified congenital malformations of respiratory system | ||
| Q34.9 | Congenital malformation of respiratory system, unspecified | ||
| Q35 | Cleft palate | ||
| Q35.0 | Cleft hard palate, bilateral | ||
| Q35.1 | Cleft hard palate, unilateral | ||
| Q35.2 | Cleft soft palate, bilateral | ||
| Q35.3 | Cleft soft palate, unilateral | ||
| Q35.4 | Cleft hard palate with cleft soft palate, bilateral | ||
| Q35.5 | Cleft hard palate with cleft soft palate, unilateral | ||
| Q35.6 | Cleft palate, medial | ||
| Q35.7 | Cleft uvula | ||
| Q35.8 | Cleft palate, unspecified, bilateral | ||
| Q35.9 | Cleft palate, unspecified, unilateral | ||
| Q36 | Cleft lip | ||
| Q36.0 | Cleft lip, bilateral | ||
| Q36.1 | Cleft lip, medial | ||
| Q36.9 | Cleft lip, unilateral | ||
| Q37 | Cleft palate with cleft lip | ||
| Q37.0 | Cleft hard palate with cleft lip, bilateral | ||
| Q37.1 | Cleft hard palate with cleft lip, unilateral | ||
| Q37.2 | Cleft soft palate with cleft lip, bilateral | ||
| Q37.3 | Cleft soft palate with cleft lip, unilateral | ||
| Q37.4 | Cleft hard and soft palate with cleft lip, bilateral | ||
| Q37.5 | Cleft hard and soft palate with cleft lip, unilateral | ||
| Q37.8 | Unspecified cleft palate with cleft lip, bilateral | ||
| Q37.9 | Unspecified cleft palate with cleft lip, unilateral | ||
| Q38 | Other congenital malformations of tongue, mouth and pharynx | ||
| Q38.0 | Congenital malformations of lips, not elsewhere classified | ||
| Q38.1 | Ankyloglossia | ||
| Q38.2 | Macroglossia | ||
| Q38.3 | Other congenital malformations of tongue | ||
| Q38.4 | Congenital malformations of salivary glands and ducts | ||
| Q38.5 | Congenital malformations of palate, not elsewhere classified | ||
| Q38.6 | Other congenital malformations of mouth | ||
| Q38.7 | Pharyngeal pouch | ||
| Q38.8 | Other congenital malformations of pharynx | ||
| Q39 | Congenital malformations of oesophagus | ||
| Q39.0 | Atresia of oesophagus without fistula | ||
| Q39.1 | Atresia of oesophagus with tracheo-oesophageal fistula | ||
| Q39.2 | Congenital tracheo-oesophageal fistula without atresia | ||
| Q39.3 | Congenital stenosis and stricture of oesophagus | ||
| Q39.4 | Oesophageal web | ||
| Q39.5 | Congenital dilatation of oesophagus | ||
| Q39.6 | Diverticulum of oesophagus | ||
| Q39.8 | Other congenital malformations of oesophagus | ||
| Q39.9 | Congenital malformation of oesophagus, unspecified | ||
| Q40 | Other congenital malformations of upper alimentary tract | ||
| Q40.0 | Congenital hypertrophic pyloric stenosis | ||
| Q40.1 | Congenital hiatus hernia | ||
| Q40.2 | Other specified congenital malformations of stomach | ||
| Q40.3 | Congenital malformation of stomach, unspecified | ||
| Q40.8 | Other specified congenital malformations of upper alimentary tract | ||
| Q40.9 | Congenital malformation of upper alimentary tract, unspecified | ||
| Q41 | Congenital absence, atresia and stenosis of small intestine | ||
| Q41.0 | Congenital absence, atresia and stenosis of duodenum | ||
| Q41.1 | Congenital absence, atresia and stenosis of jejunum | ||
| Q41.2 | Congenital absence, atresia and stenosis of ileum | ||
| Q41.8 | Congenital absence, atresia and stenosis of other specified parts ofsmall intestine | ||
| Q41.9 | Congenital absence, atresia and stenosis of small intestine, partunspecified | ||
| Q42 | Congenital absence, atresia and stenosis of large intestine | ||
| Q42.0 | Congenital absence, atresia and stenosis of rectum with fistula | ||
| Q42.1 | Congenital absence, atresia and stenosis of rectum without fistula | ||
| Q42.2 | Congenital absence, atresia and stenosis of anus with fistula | ||
| Q42.3 | Congenital absence, atresia and stenosis of anus without fistula | ||
| Q42.8 | Congenital absence, atresia and stenosis of other parts of largeintestine | ||
| Q42.9 | Congenital absence, atresia and stenosis of large intestine, partunspecified | ||
| Q43 | Other congenital malformations of intestine | ||
| Q43.0 | Meckel's diverticulum | ||
| Q43.1 | Hirschsprung's disease | ||
| Q43.2 | Other congenital functional disorders of colon | ||
| Q43.3 | Congenital malformations of intestinal fixation | ||
| Q43.4 | Duplication of intestine | ||
| Q43.5 | Ectopic anus | ||
| Q43.6 | Congenital fistula of rectum and anus | ||
| Q43.7 | Persistent cloaca | ||
| Q43.8 | Other specified congenital malformations of intestine | ||
| Q43.9 | Congenital malformation of intestine, unspecified | ||
| Q44 | Congenital malformations of gallbladder, bile ducts and liver | ||
| Q44.0 | Agenesis, aplasia and hypoplasia of gallbladder | ||
| Q44.1 | Other congenital malformations of gallbladder | ||
| Q44.2 | Atresia of bile ducts | ||
| Q44.3 | Congenital stenosis and stricture of bile ducts | ||
| Q44.4 | Choledochal cyst | ||
| Q44.5 | Other congenital malformations of bile ducts | ||
| Q44.6 | Cystic disease of liver | ||
| Q44.7 | Other congenital malformations of liver | ||
| Q45 | Other congenital malformations of digestive system | ||
| Q45.0 | Agenesis, aplasia and hypoplasia of pancreas | ||
| Q45.1 | Annular pancreas | ||
| Q45.2 | Congenital pancreatic cyst | ||
| Q45.3 | Other congenital malformations of pancreas and pancreatic duct | ||
| Q45.8 | Other specified congenital malformations of digestive system | ||
| Q45.9 | Congenital malformation of digestive system, unspecified | ||
| Q50 | Congenital malformations of ovaries, fallopian tubes and broadligaments | ||
| Q50.0 | Congenital absence of ovary | ||
| Q50.1 | Developmental ovarian cyst | ||
| Q50.2 | Congenital torsion of ovary | ||
| Q50.3 | Other congenital malformations of ovary | ||
| Q50.4 | Embryonic cyst of fallopian tube | ||
| Q50.5 | Embryonic cyst of broad ligament | ||
| Q50.6 | Other congenital malformations of fallopian tube and broad ligament | ||
| Q51 | Congenital malformations of uterus and cervix | ||
| Q51.0 | Agenesis and aplasia of uterus | ||
| Q51.1 | Doubling of uterus with doubling of cervix and vagina | ||
| Q51.2 | Other doubling of uterus | ||
| Q51.3 | Bicornate uterus | ||
| Q51.4 | Unicornate uterus | ||
| Q51.5 | Agenesis and aplasia of cervix | ||
| Q51.6 | Embryonic cyst of cervix | ||
| Q51.7 | Congenital fistulae between uterus and digestive and urinary tracts | ||
| Q51.8 | Other congenital malformations of uterus and cervix | ||
| Q51.9 | Congenital malformation of uterus and cervix, unspecified | ||
| Q52 | Other congenital malformations of female genitalia | ||
| Q52.0 | Congenital absence of vagina | ||
| Q52.1 | Doubling of vagina | ||
| Q52.2 | Congenital rectovaginal fistula | ||
| Q52.3 | Imperforate hymen | ||
| Q52.4 | Other congenital malformations of vagina | ||
| Q52.5 | Fusion of labia | ||
| Q52.6 | Congenital malformation of clitoris | ||
| Q52.7 | Other congenital malformations of vulva | ||
| Q52.8 | Other specified congenital malformations of female genitalia | ||
| Q52.9 | Congenital malformation of female genitalia, unspecified | ||
| Q53 | Undescended testicle | ||
| Q53.0 | Ectopic testis | ||
| Q53.1 | Undescended testicle, unilateral | ||
| Q53.2 | Undescended testicle, bilateral | ||
| Q53.9 | Undescended testicle, unspecified | ||
| Q54 | Hypospadias | ||
| Q54.0 | Hypospadias, balanic | ||
| Q54.1 | Hypospadias, penile | ||
| Q54.2 | Hypospadias, penoscrotal | ||
| Q54.3 | Hypospadias, perineal | ||
| Q54.4 | Congenital chordee | ||
| Q54.8 | Other hypospadias | ||
| Q54.9 | Hypospadias, unspecified | ||
| Q55 | Other congenital malformations of male genital organs | ||
| Q55.0 | Absence and aplasia of testis | ||
| Q55.1 | Hypoplasia of testis and scrotum | ||
| Q55.2 | Other congenital malformations of testis and scrotum | ||
| Q55.3 | Atresia of vas deferens | ||
| Q55.4 | Other congenital malformations of vas deferens, epididymis, seminalvesicles and prostate | ||
| Q55.5 | Congenital absence and aplasia of penis | ||
| Q55.6 | Other congenital malformations of penis | ||
| Q55.8 | Other specified congenital malformations of male genital organs | ||
| Q55.9 | Congenital malformation of male genital organ, unspecified | ||
| Q56 | Indeterminate sex and pseudohermaphroditism | ||
| Q56.0 | Hermaphroditism, not elsewhere classified | ||
| Q56.1 | Male pseudohermaphroditism, not elsewhere classified | ||
| Q56.2 | Female pseudohermaphroditism, not elsewhere classified | ||
| Q56.3 | Pseudohermaphroditism, unspecified | ||
| Q56.4 | Indeterminate sex, unspecified | ||
| Q60 | Renal agenesis and other reduction defects of kidney | ||
| Q60.0 | Renal agenesis, unilateral | ||
| Q60.1 | Renal agenesis, bilateral | ||
| Q60.2 | Renal agenesis, unspecified | ||
| Q60.3 | Renal hypoplasia, unilateral | ||
| Q60.4 | Renal hypoplasia, bilateral | ||
| Q60.5 | Renal hypoplasia, unspecified | ||
| Q60.6 | Potter's syndrome | ||
| Q61 | Cystic kidney disease | ||
| Q61.0 | Congenital single renal cyst | ||
| Q61.1 | Polycystic kidney, infantile type | ||
| Q61.2 | Polycystic kidney, adult type | ||
| Q61.3 | Polycystic kidney, unspecified | ||
| Q61.4 | Renal dysplasia | ||
| Q61.5 | Medullary cystic kidney | ||
| Q61.8 | Other cystic kidney diseases | ||
| Q61.9 | Cystic kidney disease, unspecified | ||
| Q62 | Congenital obstructive defects of renal pelvis and congenitalmalformations of ureter | ||
| Q62.0 | Congenital hydronephrosis | ||
| Q62.1 | Atresia and stenosis of ureter | ||
| Q62.2 | Congenital megaloureter | ||
| Q62.3 | Other obstructive defects of renal pelvis and ureter | ||
| Q62.4 | Agenesis of ureter | ||
| Q62.5 | Duplication of ureter | ||
| Q62.6 | Malposition of ureter | ||
| Q62.7 | Congenital vesico-uretero-renal reflux | ||
| Q62.8 | Other congenital malformations of ureter | ||
| Q63 | Other congenital malformations of kidney | ||
| Q63.0 | Accessory kidney | ||
| Q63.1 | Lobulated, fused and horseshoe kidney | ||
| Q63.2 | Ectopic kidney | ||
| Q63.3 | Hyperplastic and giant kidney | ||
| Q63.8 | Other specified congenital malformations of kidney | ||
| Q63.9 | Congenital malformation of kidney, unspecified | ||
| Q64 | Other congenital malformations of urinary system | ||
| Q64.0 | Epispadias | ||
| Q64.1 | Exstrophy of urinary bladder | ||
| Q64.2 | Congenital posterior urethral valves | ||
| Q64.3 | Other atresia and stenosis of urethra and bladder neck | ||
| Q64.4 | Malformation of urachus | ||
| Q64.5 | Congenital absence of bladder and urethra | ||
| Q64.6 | Congenital diverticulum of bladder | ||
| Q64.7 | Other congenital malformations of bladder and urethra | ||
| Q64.8 | Other specified congenital malformations of urinary system | ||
| Q64.9 | Congenital malformation of urinary system, unspecified | ||
| Q65 | Congenital deformities of hip | ||
| Q65.0 | Congenital dislocation of hip, unilateral | ||
| Q65.1 | Congenital dislocation of hip, bilateral | ||
| Q65.2 | Congenital dislocation of hip, unspecified | ||
| Q65.3 | Congenital subluxation of hip, unilateral | ||
| Q65.4 | Congenital subluxation of hip, bilateral | ||
| Q65.5 | Congenital subluxation of hip, unspecified | ||
| Q65.6 | Unstable hip | ||
| Q65.8 | Other congenital deformities of hip | ||
| Q65.9 | Congenital deformity of hip, unspecified | ||
| Q66 | Congenital deformities of feet | ||
| Q66.0 | Talipes equinovarus | ||
| Q66.1 | Talipes calcaneovarus | ||
| Q66.2 | Metatarsus varus | ||
| Q66.3 | Other congenital varus deformities of feet | ||
| Q66.4 | Talipes calcaneovalgus | ||
| Q66.5 | Congenital pes planus | ||
| Q66.6 | Other congenital valgus deformities of feet | ||
| Q66.7 | Pes cavus | ||
| Q66.8 | Other congenital deformities of feet | ||
| Q66.9 | Congenital deformity of feet, unspecified | ||
| Q67 | Congenital musculoskeletal deformities of head, face, spine andchest | ||
| Q67.0 | Facial asymmetry | ||
| Q67.1 | Compression facies | ||
| Q67.2 | Dolichocephaly | ||
| Q67.3 | Plagiocephaly | ||
| Q67.4 | Other congenital deformities of skull, face and jaw | ||
| Q67.5 | Congenital deformity of spine | ||
| Q67.6 | Pectus excavatum | ||
| Q67.7 | Pectus carinatum | ||
| Q67.8 | Other congenital deformities of chest | ||
| Q68 | Other congenital musculoskeletal deformities | ||
| Q68.0 | Congenital deformity of sternocleidomastoid muscle | ||
| Q68.1 | Congenital deformity of hand | ||
| Q68.2 | Congenital deformity of knee | ||
| Q68.3 | Congenital bowing of femur | ||
| Q68.4 | Congenital bowing of tibia and fibula | ||
| Q68.5 | Congenital bowing of long bones of leg, unspecified | ||
| Q68.8 | Other specified congenital musculoskeletal deformities | ||
| Q69 | Polydactyly | ||
| Q69.0 | Accessory finger(s) | ||
| Q69.1 | Accessory thumb(s) | ||
| Q69.2 | Accessory toe(s) | ||
| Q69.9 | Polydactyly, unspecified | ||
| Q70 | Syndactyly | ||
| Q70.0 | Fused fingers | ||
| Q70.1 | Webbed fingers | ||
| Q70.2 | Fused toes | ||
| Q70.3 | Webbed toes | ||
| Q70.4 | Polysyndactyly | ||
| Q70.9 | Syndactyly, unspecified | ||
| Q71 | Reduction defects of upper limb | ||
| Q71.0 | Congenital complete absence of upper limb(s) | ||
| Q71.1 | Congenital absence of upper arm and forearm with hand present | ||
| Q71.2 | Congenital absence of both forearm and hand | ||
| Q71.3 | Congenital absence of hand and finger(s) | ||
| Q71.4 | Longitudinal reduction defect of radius | ||
| Q71.5 | Longitudinal reduction defect of ulna | ||
| Q71.6 | Lobster-claw hand | ||
| Q71.8 | Other reduction defects of upper limb(s) | ||
| Q71.9 | Reduction defect of upper limb, unspecified | ||
| Q72 | Reduction defects of lower limb | ||
| Q72.0 | Congenital complete absence of lower limb(s) | ||
| Q72.1 | Congenital absence of thigh and lower leg with foot present | ||
| Q72.2 | Congenital absence of both lower leg and foot | ||
| Q72.3 | Congenital absence of foot and toe(s) | ||
| Q72.4 | Longitudinal reduction defect of femur | ||
| Q72.5 | Longitudinal reduction defect of tibia | ||
| Q72.6 | Longitudinal reduction defect of fibula | ||
| Q72.7 | Split foot | ||
| Q72.8 | Other reduction defects of lower limb(s) | ||
| Q72.9 | Reduction defect of lower limb, unspecified | ||
| Q73 | Reduction defects of unspecified limb | ||
| Q73.0 | Congenital absence of unspecified limb(s) | ||
| Q73.1 | Phocomelia, unspecified limb(s) | ||
| Q73.8 | Other reduction defects of unspecified limb(s) | ||
| Q74 | Other congenital malformations of limb(s) | ||
| Q74.0 | Other congenital malformations of upper limb(s), including shouldergirdle | ||
| Q74.1 | Congenital malformation of knee | ||
| Q74.2 | Other congenital malformations of lower limb(s), including pelvicgirdle | ||
| Q74.3 | Arthrogryposis multiplex congenita | ||
| Q74.8 | Other specified congenital malformations of limb(s) | ||
| Q74.9 | Unspecified congenital malformation of limb(s) | ||
| Q75 | Other congenital malformations of skull and face bones | ||
| Q75.0 | Craniosynostosis | ||
| Q75.1 | Craniofacial dysostosis | ||
| Q75.2 | Hypertelorism | ||
| Q75.3 | Macrocephaly | ||
| Q75.4 | Mandibulofacial dysostosis | ||
| Q75.5 | Oculomandibular dysostosis | ||
| Q75.8 | Other specified congenital malformations of skull and face bones | ||
| Q75.9 | Congenital malformation of skull and face bones, unspecified | ||
| Q76 | Congenital malformations of spine and bony thorax | ||
| Q76.0 | Spina bifida occulta | ||
| Q76.1 | Klippel-Feil syndrome | ||
| Q76.2 | Congenital spondylolisthesis | ||
| Q76.3 | Congenital scoliosis due to congenital bony malformation | ||
| Q76.4 | Other congenital malformations of spine, not associated withscoliosis | ||
| Q76.5 | Cervical rib | ||
| Q76.6 | Other congenital malformations of ribs | ||
| Q76.7 | Congenital malformation of sternum | ||
| Q76.8 | Other congenital malformations of bony thorax | ||
| Q76.9 | Congenital malformation of bony thorax, unspecified | ||
| Q77 | Osteochondrodysplasia with defects of growth of tubular bones andspine | ||
| Q77.0 | Achondrogenesis | ||
| Q77.1 | Thanatophoric short stature | ||
| Q77.2 | Short rib syndrome | ||
| Q77.3 | Chondrodysplasia punctata | ||
| Q77.4 | Achondroplasia | ||
| Q77.5 | Dystrophic dysplasia | ||
| Q77.6 | Chondroectodermal dysplasia | ||
| Q77.7 | Spondyloepiphyseal dysplasia | ||
| Q77.8 | Other osteochondrodysplasia with defects of growth of tubular bonesand spine | ||
| Q77.9 | Osteochondrodysplasia with defects of growth of tubular bones andspine, unspecified | ||
| Q78 | Other osteochondrodysplasias | ||
| Q78.0 | Osteogenesis imperfecta | ||
| Q78.1 | Polyostotic fibrous dysplasia | ||
| Q78.2 | Osteopetrosis | ||
| Q78.3 | Progressive diaphyseal dysplasia | ||
| Q78.4 | Enchondromatosis | ||
| Q78.5 | Metaphyseal dysplasia | ||
| Q78.6 | Multiple congenital exostoses | ||
| Q78.8 | Other specified osteochondrodysplasias | ||
| Q78.9 | Osteochondrodysplasia, unspecified | ||
| Q79 | Congenital malformations of the musculoskeletal system, notelsewhere classified | ||
| Q79.0 | Congenital diaphragmatic hernia | ||
| Q79.1 | Other congenital malformations of diaphragm | ||
| Q79.2 | Exomphalos | ||
| Q79.3 | Gastroschisis | ||
| Q79.4 | Prune belly syndrome | ||
| Q79.5 | Other congenital malformations of abdominal wall | ||
| Q79.6 | Ehlers-Danlos syndrome | ||
| Q79.8 | Other congenital malformations of musculoskeletal system | ||
| Q79.9 | Congenital malformation of musculoskeletal system, unspecified | ||
| Q80 | Congenital ichthyosis | ||
| Q80.0 | Ichthyosis vulgaris | ||
| Q80.1 | X-linked ichthyosis | ||
| Q80.2 | Lamellar ichthyosis | ||
| Q80.3 | Congenital bullous ichthyosiform erythroderma | ||
| Q80.4 | Harlequin fetus | ||
| Q80.8 | Other congenital ichthyosis | ||
| Q80.9 | Congenital ichthyosis, unspecified | ||
| Q81 | Epidermolysis bullosa | ||
| Q81.0 | Epidermolysis bullosa simplex | ||
| Q81.1 | Epidermolysis bullosa letalis | ||
| Q81.2 | Epidermolysis bullosa dystrophica | ||
| Q81.8 | Other epidermolysis bullosa | ||
| Q81.9 | Epidermolysis bullosa, unspecified | ||
| Q82 | Other congenital malformations of skin | ||
| Q82.0 | Hereditary lymphoedema | ||
| Q82.1 | Xeroderma pigmentosum | ||
| Q82.2 | Mastocytosis | ||
| Q82.3 | Incontinentia pigmenti | ||
| Q82.4 | Ectodermal dysplasia (anhidrotic) | ||
| Q82.5 | Congenital non-neoplastic naevus | ||
| Q82.8 | Other specified congenital malformations of skin | ||
| Q82.9 | Congenital malformation of skin, unspecified | ||
| Q83 | Congenital malformations of breast | ||
| Q83.0 | Congenital absence of breast with absent nipple | ||
| Q83.1 | Accessory breast | ||
| Q83.2 | Absent nipple | ||
| Q83.3 | Accessory nipple | ||
| Q83.8 | Other congenital malformations of breast | ||
| Q83.9 | Congenital malformation of breast, unspecified | ||
| Q84 | Other congenital malformations of integument | ||
| Q84.0 | Congenital alopecia | ||
| Q84.1 | Congenital morphological disturbances of hair, not elsewhereclassified | ||
| Q84.2 | Other congenital malformations of hair | ||
| Q84.3 | Anonychia | ||
| Q84.4 | Congenital leukonychia | ||
| Q84.5 | Enlarged and hypertrophic nails | ||
| Q84.6 | Other congenital malformations of nails | ||
| Q84.8 | Other specified congenital malformations of integument | ||
| Q84.9 | Congenital malformation of integument, unspecified | ||
| Q85 | Phakomatoses, not elsewhere classified | ||
| Q85.0 | Neurofibromatosis (nonmalignant) | ||
| Q85.1 | Tuberous sclerosis | ||
| Q85.8 | Other phakomatoses, not elsewhere classified | ||
| Q85.9 | Phakomatosis, unspecified | ||
| Q86 | Congenital malformation syndromes due to known exogenous causes, notelsewhere classified | ||
| Q86.0 | Fetal alcohol syndrome (dysmorphic) | ||
| Q86.1 | Fetal hydantoin syndrome | ||
| Q86.2 | Dysmorphism due to warfarin | ||
| Q86.8 | Other congenital malformation syndromes due to known exogenouscauses | ||
| Q87 | Other specified congenital malformation syndromes affecting multiplesystems | ||
| Q87.0 | Congenital malformation syndromes predominantly affecting facialappearance | ||
| Q87.1 | Congenital malformation syndromes predominantly associated withshort stature | ||
| Q87.2 | Congenital malformation syndromes predominantly involving limbs | ||
| Q87.3 | Congenital malformation syndromes involving early overgrowth | ||
| Q87.4 | Marfan's syndrome | ||
| Q87.5 | Other congenital malformation syndromes with other skeletal changes | ||
| Q87.8 | Other specified congenital malformation syndromes, not elsewhereclassified | ||
| Q89 | Other congenital malformations, not elsewhere classified | ||
| Q89.0 | Congenital malformations of spleen | ||
| Q89.1 | Congenital malformations of adrenal gland | ||
| Q89.2 | Congenital malformations of other endocrine glands | ||
| Q89.3 | Situs inversus | ||
| Q89.4 | Conjoined twins | ||
| Q89.7 | Multiple congenital malformations, not elsewhere classified | ||
| Q89.8 | Other specified congenital malformations | ||
| Q89.9 | Congenital malformation, unspecified | ||
| Q90 | Down's syndrome | ||
| Q90.0 | Trisomy 21, meiotic nondisjunction | ||
| Q90.1 | Trisomy 21, mosaicism (mitotic nondisjunction) | ||
| Q90.2 | Trisomy 21, translocation | ||
| Q90.9 | Down's syndrome, unspecified | ||
| Q91 | Edwards' syndrome and Patau's syndrome | ||
| Q91.0 | Trisomy 18, meiotic nondisjunction | ||
| Q91.1 | Trisomy 18, mosaicism (mitotic nondisjunction) | ||
| Q91.2 | Trisomy 18, translocation | ||
| Q91.3 | Edwards' syndrome, unspecified | ||
| Q91.4 | Trisomy 13, meiotic nondisjunction | ||
| Q91.5 | Trisomy 13, mosaicism (mitotic nondisjunction) | ||
| Q91.6 | Trisomy 13, translocation | ||
| Q91.7 | Patau's syndrome, unspecified | ||
| Q92 | Other trisomies and partial trisomies of the autosomes, notelsewhere classified | ||
| Q92.0 | Whole chromosome trisomy, meiotic nondisjunction | ||
| Q92.1 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) | ||
| Q92.2 | Major partial trisomy | ||
| Q92.3 | Minor partial trisomy | ||
| Q92.4 | Duplications seen only at prometaphase | ||
| Q92.5 | Duplications with other complex rearrangements | ||
| Q92.6 | Extra marker chromosomes | ||
| Q92.7 | Triploidy and polyploidy | ||
| Q92.8 | Other specified trisomies and partial trisomies of autosomes | ||
| Q92.9 | Trisomy and partial trisomy of autosomes, unspecified | ||
| Q93 | Monosomies and deletions from the autosomes, not elsewhereclassified | ||
| Q93.0 | Whole chromosome monosomy, meiotic nondisjunction | ||
| Q93.1 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) | ||
| Q93.2 | Chromosome replaced with ring or dicentric | ||
| Q93.3 | Deletion of short arm of chromosome 4 | ||
| Q93.4 | Deletion of short arm of chromosome 5 | ||
| Q93.5 | Other deletions of part of a chromosome | ||
| Q93.6 | Deletions seen only at prometaphase | ||
| Q93.7 | Deletions with other complex rearrangements | ||
| Q93.8 | Other deletions from the autosomes | ||
| Q93.9 | Deletion from autosomes, unspecified | ||
| Q95 | Balanced rearrangements and structural markers, not elsewhereclassified | ||
| Q95.0 | Balanced translocation and insertion in normal individual | ||
| Q95.1 | Chromosome inversion in normal individual | ||
| Q95.2 | Balanced autosomal rearrangement in abnormal individual | ||
| Q95.3 | Balanced sex/autosomal rearrangement in abnormal individual | ||
| Q95.4 | Individuals with marker heterochromatin | ||
| Q95.5 | Individuals with autosomal fragile site | ||
| Q95.8 | Other balanced rearrangements and structural markers | ||
| Q95.9 | Balanced rearrangement and structural marker, unspecified | ||
| Q96 | Turner's syndrome | ||
| Q96.0 | Karyotype 45,X | ||
| Q96.1 | Karyotype 46,X iso (Xq) | ||
| Q96.2 | Karyotype 46,X with abnormal sex chromosome, except iso (Xq) | ||
| Q96.3 | Mosaicism, 45,X/46,XX or XY | ||
| Q96.4 | Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome | ||
| Q96.8 | Other variants of Turner's syndrome | ||
| Q96.9 | Turner's syndrome, unspecified | ||
| Q97 | Other sex chromosome abnormalities, female phenotype, not elsewhereclassified | ||
| Q97.0 | Karyotype 47,XXX | ||
| Q97.1 | Female with more than three X chromosomes | ||
| Q97.2 | Mosaicism, lines with various numbers of X chromosomes | ||
| Q97.3 | Female with 46,XY karyotype | ||
| Q97.8 | Other specified sex chromosome abnormalities, female phenotype | ||
| Q97.9 | Sex chromosome abnormality, female phenotype, unspecified | ||
| Q98 | Other sex chromosome abnormalities, male phenotype, not elsewhereclassified | ||
| Q98.0 | Klinefelter's syndrome karyotype 47,XXY | ||
| Q98.1 | Klinefelter's syndrome, male with more than two X chromosomes | ||
| Q98.2 | Klinefelter's syndrome, male with 46,XX karyotype | ||
| Q98.3 | Other male with 46,XX karyotype | ||
| Q98.4 | Klinefelter's syndrome, unspecified | ||
| Q98.5 | Karyotype 47,XYY | ||
| Q98.6 | Male with structurally abnormal sex chromosome | ||
| Q98.7 | Male with sex chromosome mosaicism | ||
| Q98.8 | Other specified sex chromosome abnormalities, male phenotype | ||
| Q98.9 | Sex chromosome abnormality, male phenotype, unspecified | ||
| Q99 | Other chromosome abnormalities, not elsewhere classified | ||
| Q99.0 | Chimera 46,XX/46,XY | ||
| Q99.1 | 46,XX true hermaphrodite | ||
| Q99.2 | Fragile X chromosome | ||
| Q99.8 | Other specified chromosome abnormalities | ||
| Q99.9 | Chromosomal abnormality, unspecified |
Jumat, 11 Juli 2014
Congenital malformations, deformations, & chromosomal abnormalities
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