International Classification of Diseases, 11th Edition, China

Last uploaded: November 11, 2019

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

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/ICD10CM/E70.2	International Classification of Diseases, Version 10 - Clinical Modification	LOOM
	http://purl.bioontology.org/ontology/ICD10/E70.2	International Classification of Diseases, Version 10	LOOM