Preferred Name

遗传性共济失调 / Hereditary ataxia

Definitions

A group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements

ID

http://purl.bmicc.cn/ontology/ICD11CN/8A03.1

definition

A group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements

exclusions

Cerebral palsy (BlockL1‑8D2)

Metabolic disorders (BlockL1‑5C5)

free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/G11

has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/G11

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/442347652

label

遗传性共济失调 / Hereditary ataxia

notation

8A03.1

prefixIRI

ICD11CN:A03.1

prefLabel

遗传性共济失调 / Hereditary ataxia

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/8A03

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http://purl.obolibrary.org/obo/DOID_0050951 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/ICD10/G11 International Classification of Diseases, Version 10 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G11 International Classification of Diseases, Version 10 - Clinical Modification LOOM