spinocerebellar ataxia type 13
Human disease
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spinocerebellar ataxia type 13
Summary
spinocerebellar ataxia type 13 is a developmental defect during embryogenesis[1]. It draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]
Key Facts
- spinocerebellar ataxia type 13's instance of is recorded as developmental defect during embryogenesis[3].
- spinocerebellar ataxia type 13's instance of is recorded as rare disease[4].
- spinocerebellar ataxia type 13's instance of is recorded as class of disease[5].
- spinocerebellar ataxia type 13's subclass of is recorded as spinocerebellar ataxia[6].
- spinocerebellar ataxia type 13's subclass of is recorded as autosomal dominant cerebellar ataxia type I[7].
- spinocerebellar ataxia type 13's MeSH descriptor ID is recorded as C537195[8].
- spinocerebellar ataxia type 13's OMIM ID is recorded as 605259[9].
- spinocerebellar ataxia type 13's ICD-9 ID is recorded as 334.9[10].
- spinocerebellar ataxia type 13's ICD-10 ID is recorded as G11.2[11].
- spinocerebellar ataxia type 13's DiseasesDB is recorded as 12339[12].
- spinocerebellar ataxia type 13's eMedicine ID is recorded as 1153370[13].
- spinocerebellar ataxia type 13's Disease Ontology ID is recorded as DOID:0050963[14].
- spinocerebellar ataxia type 13's Orphanet ID is recorded as 98768[15].
- spinocerebellar ataxia type 13's health specialty is recorded as neurology[16].
- spinocerebellar ataxia type 13's genetic association is recorded as KCNC3[17].
- spinocerebellar ataxia type 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050963[18].
- spinocerebellar ataxia type 13's exact match is recorded as http://identifiers.org/doid/DOID:0050963[19].
- spinocerebellar ataxia type 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98768[20].
- spinocerebellar ataxia type 13's UMLS CUI is recorded as C1854488[21].
- spinocerebellar ataxia type 13's ICD-10-CM is recorded as G11.2[22].
- spinocerebellar ataxia type 13's GARD rare disease ID is recorded as 9611[23].
- spinocerebellar ataxia type 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
- spinocerebellar ataxia type 13's Mondo ID is recorded as MONDO_0011529[25].
- spinocerebellar ataxia type 13's SNOMED CT ID is recorded as 719209002[26].
- spinocerebellar ataxia type 13's Microsoft Academic ID is recorded as 2776395606[27].
Why It Matters
spinocerebellar ataxia type 13 draws 4 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]