ICD-10 అధ్యాయము 17: వంశపారంపరిక అవలక్షణాలు మరియు జన్యు సంబంధ వ్యాధులు
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[మార్చు] Q00-Q89 - Congenital malformations and deformations
[మార్చు] (Q00-Q07) నరముల వ్యవస్థ
- (Q00.) Anencephaly and similar malformations
- (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
- Agyria and Lissencephaly (EUROCAT Q04.33)
- Microgyria and Pachygyria (EUROCAT Q04.34)
- Hydranencephaly (EUROCAT Q04.35)
- (Q04.4) Septo-optic dysplasia
- (Q04.5) Megalencephaly
- (Q04.6) Congenital cerebral cysts
- Porencephaly
- Schizencephaly
- (Q04.8) Other specified congenital malformations of brain
- (Q04.9) Congenital malformation of brain, unspecified
- (Q05.) Spina bifida
- (Q06.) Other congenital malformations of spinal cord
- (Q07.) Other congenital malformations of nervous system
[మార్చు] (Q10-Q18) కన్ను, చెవి, ముఖము మరియు మెడ
- (Q10.) కంటిగుడ్డుకు చెందిన జన్యులోపములు, 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
- (Q12.) Congenital lens malformations
- (Q13.) Congenital malformations of anterior segment of eye
- (Q13.1) Absence of iris
- Aniridia
- (Q13.1) Absence of iris
- (Q14.) Congenital malformations of posterior segment of eye
- (Q15.) Other congenital malformations of eye
- (Q15.0) Congenital glaucoma
- Buphthalmos
- Glaucoma of newborn
- Hydrophthalmos
- Keratoglobus, congenital, with glaucoma
- Macrocornea with glaucoma
- Macrophthalmos in congenital glaucoma
- Megalocornea with glaucoma
- (Q15.0) Congenital glaucoma
- (Q16.) Congenital malformations of ear causing impairment of hearing
- (Q17.) Other congenital malformations of ear
- (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
- Otocephaly
- (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
[మార్చు] (Q20-Q28) ప్రసరణ వ్యవస్థ
- (Q20.) గుండెగదులుమరియు అనుసంధానములలో జన్యులోపములుmadhu
- (Q20.0) Common arterial trunk
- Persistent truncus arteriosus
- (Q20.1) Double outlet right ventricle
- Taussig-Bing syndrome
- (Q20.2) Double outlet left ventricle
- (Q20.3) Discordant ventriculoarterial connection
- Dextrotransposition of aorta
- Transposition of great vessels (complete)
- (Q20.4) Double inlet ventricle
- (Q20.5) Discordant atrioventricular connection
- Corrected transposition
- (Q20.6) Isomerism of atrial appendages
- (Q20.0) Common arterial trunk
- (Q21.) Congenital malformations of cardiac septa
- (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
- Tricuspid atresia
- (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
- (Q25.4) Other congenital malformations of aorta
- Overriding aorta (EUROCAT Q25.42)
- Aneurysm of sinus of Valsalva (ruptured) (EUROCAT Q25.43)
- (Q25.5) Atresia of pulmonary artery
- (Q25.6) Stenosis of pulmonary artery
- (Q25.7) Other congenital malformations of pulmonary artery
- (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
- Scimitar syndrome
- (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 vascular system
- (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
[మార్చు] (Q30-Q34) శ్వాస వ్యవస్థ
- (Q31.) Congenital malformations of larynx
- (Q32.) Congenital malformations of trachea and 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
[మార్చు] (Q35-Q45) జీర్ణ వ్యవస్థ
- (Q35.) Cleft palate
- (Q36.) Cleft lip
- (Q37.) Cleft palate with cleft lip
- (Q38.) Other congenital malformations of tongue, mouth and pharynx
- (Q38.0) Congenital malformations of lips, not elsewhere classified
- Van der Woude's syndrome
- (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
- (Q38.0) Congenital malformations of lips, not elsewhere classified
- (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
- (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 of small intestine
- (Q41.9) Congenital absence, atresia and stenosis of small intestine, part unspecified
- (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
- Imperforate rectum
- (Q42.2) Congenital absence, atresia and stenosis of anus with fistula
- (Q42.3) Congenital absence, atresia and stenosis of anus without fistula
- Imperforate anus
- (Q42.8) Congenital absence, atresia and stenosis of other parts of large intestine
- (Q42.9) Congenital absence, atresia and stenosis of large intestine, part unspecified
- (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
- (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
- Accessory liver
- Alagille's syndrome
- (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]]
[మార్చు] (Q50-Q56) జననావయవాలు
- (Q50.) Congenital malformations of ovaries, fallopian tubes and broad ligaments
- (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
- (Q55.) Other congenital malformations of male genital organs
- (Q56.) Indeterminate sex and pseudohermaphroditism
[మార్చు] (Q60-Q64) మూత్ర వ్యవస్థ
- (Q60.) Renal agenesis and other reduction defects of kidney
- (Q61.) Cystic kidney disease
- (Q62.) Congenital obstructive defects of renal pelvis and congenital malformations of ureter
- (Q63.) Other congenital malformations of kidney
- (Q64.) మూత్ర వ్యవస్థకు సంబంధించిన ఇతర జన్యులోపములుmadhu
- (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
- Cyst of urachus
- Patent urachus
- Prolapse 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
[మార్చు] (Q65-Q79) musculoskeletal system
- (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 and 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
- (Q70.) Syndactyly
- (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
- (Q74.) Other congenital malformations of limb(s)
- (Q74.0) Other congenital malformations of upper limb(s), including shoulder girdle
- Accessory carpal bones
- Cleidocranial dysostosis
- Congenital pseudarthrosis of clavicle
- Macrodactylia (fingers)
- Madelung's deformity
- Radioulnar synostosis
- Sprengel's deformity
- Triphalangeal thumb
- (Q74.1) Congenital malformation of knee
- (Q74.2) Other congenital malformations of lower limb(s), including pelvic girdle
- (Q74.3) Arthrogryposis multiplex congenita
- (Q74.8) Other specified congenital malformations of limb(s)
- (Q74.9) Unspecified congenital malformation of limb(s)
- (Q74.0) Other congenital malformations of upper limb(s), including shoulder girdle
- (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
- Franceschetti syndrome
- Treacher-Collins syndrome
- (Q75.5) Oculomandibular dysostosis
- (Q75.8) Other specified congenital malformations of skull and face bones
- Absence of skull bone, congenital
- Congenital deformity of forehead
- Platybasia
- (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 with scoliosis
- (Q76.5) Cervical rib
- (Q76.6) Other congenital malformations of ribs
- (Q76.7) Congenital malformation of sternum
- Congenital absence of sternum
- Sternum bifidum
- (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 and spine
- (Q77.0) Achondrogenesis
- (Q77.1) Thanatophoric short stature
- (Q77.2) Short rib syndrome
- (Q77.3) Chondrodysplasia punctata
- (Q77.4) Achondroplasia
- Hypochondroplasia
- (Q77.5) Dystrophic dysplasia
- (Q77.6) Chondroectodermal dysplasia
- Ellis-van Creveld syndrome
- (Q77.7) Spondyloepiphyseal dysplasia
- (Q77.8) Other osteochondrodysplasia with defects of growth of tubular bones and spine
- (Q77.9) Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
- (Q78.) Other osteochondrodysplasias
- (Q78.0) Osteogenesis imperfecta
- (Q78.1) Polyostotic fibrous dysplasia
- (Q78.2) Osteopetrosis
- (Q78.3) Progressive diaphyseal dysplasia
- (Q78.4) Enchondromatosis
- Maffucci's syndrome
- Ollier's disease
- (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, not elsewhere classified
- (Q79.0) Congenital diaphragmatic hernia
- (Q79.1) Other congenital malformations of diaphragm
- (Q79.2) Exomphalos
- Omphalocele
- (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
[మార్చు] (Q80-Q89) ఇతరము
- (Q80.) Congenital ichthyosis
- (Q81.) Epidermolysis bullosa
- (Q82.) చర్మముకు సంబంధించిన ఇతర జన్యులోపములు
- (Q82.0) Hereditary lymphoedema
- (Q82.1) Xeroderma pigmentosum
- (Q82.2) Mastocytosis
- Urticaria pigmentosa
- (Q82.3) Incontinentia pigmenti
- (Q82.4) Ectodermal dysplasia (anhidrotic)
- (Q82.5) Congenital non-neoplastic naevus
- Birthmark NOS
- naevus flammeus / Port-wine stain
- sanguineous naevus
- strawberry naevus
- vascular naevus NOS
- verrucous naevus
- (Q82.8) Other specified congenital malformations of skin
- Abnormal palmar creases
- Accessory skin tags
- Benign familial pemphigus (Hailey-Hailey)
- Cutis laxa (hyperelastica)
- Dermatoglyphic anomalies
- Inherited keratosis palmaris et plantaris
- Keratosis follicularis (Darier-White) (ILDS Q82.868)
- (Q82.9) Congenital malformation of skin, unspecified
- (Q83.) Congenital malformations of breast
- (Q84.) Other congenital malformations of integument
-
- (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)
- Von Recklinghausen's disease (ILDS Q85.010)
- Neurofibromatosis II (ILDS Q85.020)
- Neurofibromatosis, segmental (ILDS Q85.030)
- (Q85.1) Tuberous sclerosis
- Bourneville's disease
- (Q85.8) Other phakomatoses, not elsewhere classified
- Sturge-Weber syndrome (EUROCAT Q85.81)
- von Hippel-Lindau disease (EUROCAT Q85.82)
- (Q85.9) Phakomatosis, unspecified
- Hamartosis NOS
- (Q85.0) Neurofibromatosis (nonmalignant)
- (Q86.) Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
- (Q86.0) Fetal alcohol syndrome (dysmorphic)
- (Q87.) Other specified congenital malformation syndromes affecting multiple systems
- (Q87.0) Congenital malformation syndromes predominantly affecting facial appearance
- Acrocephalopolysyndactyly
- Acrocephalosyndactyly (Apert)
- Cryptophthalmos syndrome
- Cyclopia
- Goldenhar syndrome
- Moebius syndrome
- oro-facial-digital syndrome
- Robin syndrome
- Whistling face
- (Q87.0) Congenital malformation syndromes predominantly affecting facial appearance
-
- (Q87.1) Congenital malformation syndromes predominantly associated with short stature
- Aarskog syndrome
- Cockayne syndrome (ILDS Q87.110)
- De Lange syndrome (ILDS Q87.170)
- Dubowitz syndrome
- Noonan syndrome
- Prader-Willi syndrome
- Robinow-Silverman-Smith syndrome
- Silver-Russell syndrome (ILDS Q87.114)
- Seckel syndrome
- Smith-Lemli-Opitz syndrome
- Sjögren-Larsson syndrome (ILDS Q87.136)
- (Q87.2) Congenital malformation syndromes predominantly involving limbs
- Holt-Oram syndrome
- Klippel-Trénaunay-Weber (EUROCAT Q87.21, ILDS Q87.210)
- Nail-patella syndrome (ILDS Q87.230)
- Rubinstein-Taybi syndrome (EUROCAT Q87.23)
- sirenomelia
- thrombocytopenia with absent radius syndrome
- VATER syndrome
- (Q87.3) Congenital malformation syndromes involving early overgrowth
- Beckwith-Wiedemann syndrome
- Sotos syndrome
- Weaver syndrome
- (Q87.4) Marfan's syndrome
- (Q87.5) Other congenital malformation syndromes with other skeletal changes
- (Q87.8) Other specified congenital malformation syndromes, not elsewhere classified
- Alport syndrome (EUROCAT Q87.80)
- Bardet-Biedl syndrome (EUROCAT Q87.81)
- Zellweger's syndrome (EUROCAT Q87.83)
- William's syndrome (EUROCAT Q87.84)
- Angelman's syndrome (Happy puppet syndrome) (EUROCAT Q87.85)
- (Q87.1) Congenital malformation syndromes predominantly associated with short stature
- (Q89.) Other congenital malformations, not elsewhere classified
- (Q89.0) Congenital malformations of spleen
- Asplenia (congenital)
- Congenital splenomegaly
- (Q89.1) Congenital malformations of adrenal gland
- (Q89.2) Congenital malformations of other endocrine glands
- Congenital malformation of parathyroid or thyroid gland
- Persistent thyroglossal duct
- Thyroglossal cyst
- (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
- (Q89.0) Congenital malformations of spleen
[మార్చు] Q90-Q99 - క్రోమోజోముల అసాధారణతలు, వేరెక్కడనూ వర్గీకరించబడనివి
- (Q90.) Down's syndrome
- (Q91.) Trisomy 18 and Trisomy 13
- (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, not elsewhere classified
- Trisomy 9
- Warkany syndrome 2
- (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 elsewhere classified
- (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
- Wolff-Hirschorn syndrome
- (Q93.4) Deletion of short arm of chromosome 5
- Cri-du-chat syndrome
- (Q93.5) Other deletions of part of a chromosome
- Angelman syndrome
- (Q93.6) Deletion 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 elsewhere classified
- Robertsonian and balanced reciprocal translocations and insertions
- (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 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 elsewhere classified
- (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 elsewhere classified
- (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
[మార్చు] ఇవి కూడా చూడండి
- ICD-10 సంకేతముల జాబితా
- International Statistical Classification of Diseases and Related Health Problems
- List of ICD-9 codes 740-759: Congenital anomalies
- జన్యు సమస్య (Congenital disorder)
మూస:Congenital malformations and deformations of nervous system మూస:Congenital malformations and deformations of eye, ear, face and neck మూస:Congenital malformations and deformations of circulatory system మూస:Congenital malformations and deformations of respiratory system మూస:Congenital malformations and deformations of digestive system మూస:Congenital malformations of genital organs and urinary system మూస:Congenital malformations and deformations of musculoskeletal system మూస:Congenital malformations and deformations of integument మూస:Phakomatoses and other congenital malformations not elsewhere classified మూస:Chromosomal abnormalities
