|
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
|
||
Kamis, 01 Mei 2014
Q00-99
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