ICD-11 บทที่ 20 ความผิดปกติแต่กำเนิด


[การค้นหารหัส ICD-11 อาจใช้เครื่องมือ ICD-11 Browser ซึ่งสะดวกกว่าการเปิดค้นหาจากหนังสือ]

https://icd.who.int/browse11/l-m/en

# Structural developmental anomalies primarily affecting one body system  

 Structural developmental anomalies of the eye, eyelid or lacrimal apparatus  
 Structural developmental anomalies of the ear  
 Structural developmental anomalies of the face, mouth or teeth  
 Structural developmental anomalies of the neck  
 Structural developmental anomalies of the respiratory system  
 Structural developmental anomalies of the circulatory system  
 Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord  
 Structural developmental anomalies of the digestive tract  
 Structural developmental anomalies of the liver, biliary tract, pancreas or spleen  
 Structural developmental anomalies of the urinary system  
 Structural developmental anomalies of the female genital system  
 Structural developmental anomalies of the male genital system  
 Structural developmental anomalies of the breast  
 Structural developmental anomalies of the skeleton  
 Structural developmental anomalies of the skin  
 Structural developmental anomalies of the adrenal glands  
LD0Y Other specified structural developmental anomalies primarily affecting one body system  
LD0Z Structural developmental anomalies primarily affecting one body system, unspecified  

# Multiple developmental anomalies or syndromes  

LD20 Syndromes with central nervous system anomalies as a major feature  
LD21 Syndromes with eye anomalies as a major feature  
LD22 Syndromes with dental anomalies as a major feature  
LD23 Syndromes with vascular anomalies as a major feature  
LD24 Syndromes with skeletal anomalies as a major feature  
LD25 Syndromes with face or limb anomalies as a major feature  
LD26 Syndromes with limb anomalies as a major feature  
LD27 Syndromes with skin or mucosal anomalies as a major feature  
LD28 Syndromes with connective tissue involvement as a major feature  
LD29 Syndromes with obesity as a major feature  
LD2A Malformative disorders of sex development  
LD2B Syndromes with premature ageing appearance as a major feature  
LD2C Overgrowth syndromes  
LD2D Phakomatoses or hamartoneoplastic syndromes  
LD2E Syndromes with structural anomalies due to inborn errors of metabolism  
LD2F Syndromes with multiple structural anomalies, without predominant body system involvement  
LD2G Conjoined twins  
LD2H Syndromic genetic deafness  
LD2Y Other specified multiple developmental anomalies or syndromes  
LD2Z Multiple developmental anomalies or syndromes, unspecified 

# Chromosomal anomalies, excluding gene mutations  

LD40 Complete trisomies of the autosomes  
LD41 Duplications of the autosomes  
LD42 Polyploidies  
LD43 Complete monosomies of the autosomes  
LD44 Deletions of the autosomes  
LD45 Uniparental disomies  
LD46 Imprinting errors  
LD47 Balanced rearrangements or structural markers  
 Sex chromosome anomalies  
LD7Y Other specified chromosomal anomalies, excluding gene mutations  
LD7Z Chromosomal anomalies, excluding gene mutations, unspecified  

# LD90 Conditions with disorders of intellectual development as a relevant clinical feature  

LD90.0 Angelman syndrome  
LD90.1 Early-onset parkinsonism - intellectual deficit  
LD90.2 Pelizaeus-Merzbacher-like disease  
LD90.3 Prader-Willi syndrome  
LD90.4 Rett syndrome  
5C55.01 Lesch-Nyhan syndrome  
LA04.0 Hydrocephalus with stenosis of the aqueduct of Sylvius  
8A44.0 Pelizaeus-Merzbacher disease  
8C21.2 Hereditary sensory and autonomic neuropathy type IV  
LD20.00 Joubert syndrome  
5C50.0 Phenylketonuria  
5C50.12 Tyrosinaemia type 2  
5C50.A1 Carbamoylphosphate synthetase deficiency  
5C50.F1 Carnosinaemia  
5C50.F2 Homocarnosinosis  
LD20.1 Syndromes with lissencephaly as a major feature  
5C52.03 Sjögren-Larsson syndrome  
LA05.50 Polymicrogyria  
LA05.60 Porencephaly  
5C53.02 Pyruvate dehydrogenase complex deficiency  
CB04.5 Brain-lung-thyroid syndrome  
5C56.02 Metachromatic leukodystrophy  
5C56.1 Neuronal ceroid lipofuscinosis  
5C56.31 Mucopolysaccharidosis type 2  
5C56.33 Mucopolysaccharidosis type 6  
5C60.0 Oculocerebrorenal syndrome  
LD44.N0 CATCH 22 phenotype  
LD24.80 Langer-Giedion syndrome  
5C58.00 Crigler-Najjar syndrome  
LD55 Fragile X chromosome  
LD27.00 Incontinentia pigmenti  
LD2D.2 Tuberous sclerosis  
LD2F.15 Noonan syndrome  
KA62.8 Congenital rubella syndrome  
KA62.3 Congenital cytomegalovirus infection  
LD40.0 Complete trisomy 21  
LD50.31 Klinefelter syndrome, male with more than two X chromosomes  
LD90.Y Other specified conditions with disorders of intellectual development as a relevant clinical feature  
LD90.Z Conditions with disorders of intellectual development as a relevant clinical feature, unspecified  
# LD9Y Other specified developmental anomalies    
# LD9Z Developmental anomalies, unspecified    

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ลิงค์ที่เกี่ยวข้อง

ICD-11 การจัดกลุ่ม และจำแนกโรค ขององค์การอนามัยโลก

https://www.gotoknow.org/posts/703825

 

 

 

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