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Preferred Name

支链氨基酸代谢紊乱 / Disorders of branched-chain amino acid metabolism
ID

http://purl.bmicc.cn/ontology/ICD11CN/5C50.D
exclusions

Propionic acidaemia (5C50.E0)

3-methylglutaconic aciduria (5C50.E0)

Isovaleric acidaemia (5C50.E0)

3-hydroxyisobutyric aciduria (5C50.E0)

Developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency (5C50.E0)

Methylmalonic acidaemia (5C50.E0)
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/5456505
label

支链氨基酸代谢紊乱 / Disorders of branched-chain amino acid metabolism
mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/E71.2
notation

5C50.D
prefixIRI

ICD11CN:C50.D
prefLabel

支链氨基酸代谢紊乱 / Disorders of branched-chain amino acid metabolism
subClassOf

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