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Preferred Name

肌营养不良 / Muscular dystrophy
Definitions

Progressive, hereditary skeletal muscle diseases characterized by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and fatty tissue.
ID

http://purl.bmicc.cn/ontology/ICD11CN/8C70
Coded_Elsewhere

Muscular dystrophy affecting extraocular muscle (9C82.1)

Epidermolysis bullosa simplex with muscular dystrophy (EC30)

Barth syndrome (5C50.E0)
definition

Progressive, hereditary skeletal muscle diseases characterized by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and fatty tissue.
free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/G71.0
has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/G71.0
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/1464662404
label

肌营养不良 / Muscular dystrophy
notation

8C70
prefixIRI

ICD11CN:C70
prefLabel

肌营养不良 / Muscular dystrophy
subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/L2-8C7
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_9884 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/ICD10/G71.0 International Classification of Diseases, Version 10 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037519 Online Mendelian Inheritance in Man LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84910 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/ICD10CM/G71.0 International Classification of Diseases, Version 10 - Clinical Modification LOOM