hereditary ataxia
neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements
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hereditary ataxia
Summary
hereditary ataxia is a class of disease[1].
Key Facts
- hereditary ataxia's instance of is recorded as class of disease[2].
- hereditary ataxia's subclass of is recorded as neurodegeneration[3].
- hereditary ataxia's Disease Ontology ID is recorded as DOID:0050951[4].
- hereditary ataxia's Orphanet ID is recorded as 183518[5].
- hereditary ataxia's NCI Thesaurus ID is recorded as C140268[6].
- hereditary ataxia's Google Knowledge Graph ID is recorded as /g/120zjr9z[7].
- hereditary ataxia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050951[8].
- hereditary ataxia's exact match is recorded as http://identifiers.org/doid/DOID:0050951[9].
- hereditary ataxia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_183518[10].
- hereditary ataxia's UMLS CUI is recorded as C0004138[11].
- hereditary ataxia's UMLS CUI is recorded as C5680563[12].
- hereditary ataxia's ICD-10-CM is recorded as G11[13].
- hereditary ataxia's GARD rare disease ID is recorded as 6614[14].
- hereditary ataxia's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- hereditary ataxia's Mondo ID is recorded as MONDO_0000557[16].
- hereditary ataxia's ICD-11 ID is recorded as 8A03.1[17].
- hereditary ataxia's ICD-11 ID is recorded as 442347652[18].
- hereditary ataxia's Experimental Factor Ontology ID is recorded as 0009671[19].