spinocerebellar ataxia type 26

Summary

spinocerebellar ataxia type 26 is a developmental defect during embryogenesis^[1].

Key Facts

• spinocerebellar ataxia type 26's instance of is recorded as developmental defect during embryogenesis^[2].
• spinocerebellar ataxia type 26's instance of is recorded as rare disease^[3].
• spinocerebellar ataxia type 26's instance of is recorded as class of disease^[4].
• spinocerebellar ataxia type 26's subclass of is recorded as spinocerebellar ataxia^[5].
• spinocerebellar ataxia type 26's subclass of is recorded as autosomal dominant cerebellar ataxia type III^[6].
• spinocerebellar ataxia type 26's MeSH descriptor ID is recorded as C537203^[7].
• spinocerebellar ataxia type 26's OMIM ID is recorded as 609306^[8].
• spinocerebellar ataxia type 26's Disease Ontology ID is recorded as DOID:0050975^[9].
• spinocerebellar ataxia type 26's Orphanet ID is recorded as 101112^[10].
• spinocerebellar ataxia type 26's genetic association is recorded as EEF2^[11].
• spinocerebellar ataxia type 26's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050975^[12].
• spinocerebellar ataxia type 26's exact match is recorded as http://identifiers.org/doid/DOID:0050975^[13].
• spinocerebellar ataxia type 26's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101112^[14].
• spinocerebellar ataxia type 26's UMLS CUI is recorded as C1836395^[15].
• spinocerebellar ataxia type 26's ICD-10-CM is recorded as G11.2^[16].
• spinocerebellar ataxia type 26's GARD rare disease ID is recorded as 9995^[17].
• spinocerebellar ataxia type 26's on focus list of Wikimedia project is recorded as WikiProject Medicine^[18].
• spinocerebellar ataxia type 26's Mondo ID is recorded as MONDO_0012246^[19].
• spinocerebellar ataxia type 26's UniProt disease ID is recorded as DI-03933^[20].