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Preferred Name

酪氨酸代谢紊乱 / Disorders of tyrosine metabolism
ID

http://purl.bmicc.cn/ontology/ICD11CN/5C50.1
Coded_Elsewhere

Autosomal recessive dopa-responsive dystonia (8A02.11)

Oculocutaneous albinism type 1A (EC23.20)

Oculocutaneous albinism type 1B (EC23.20)
free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/E70.2
has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/E70.2
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/1842978338
label

酪氨酸代谢紊乱 / Disorders of tyrosine metabolism
notation

5C50.1
prefixIRI

ICD11CN:C50.1
prefLabel

酪氨酸代谢紊乱 / Disorders of tyrosine metabolism
subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/5C50
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http://purl.bioontology.org/ontology/ICD10CM/E70.2 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/ICD10/E70.2 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM