spinocerebellar ataxia type 35

Summary

spinocerebellar ataxia type 35 is a developmental defect during embryogenesis^[1].

Key Facts

• spinocerebellar ataxia type 35's instance of is recorded as developmental defect during embryogenesis^[2].
• spinocerebellar ataxia type 35's instance of is recorded as rare disease^[3].
• spinocerebellar ataxia type 35's instance of is recorded as class of disease^[4].
• spinocerebellar ataxia type 35's subclass of is recorded as spinocerebellar ataxia^[5].
• spinocerebellar ataxia type 35's subclass of is recorded as autosomal dominant cerebellar ataxia type I^[6].
• spinocerebellar ataxia type 35's OMIM ID is recorded as 613908^[7].
• spinocerebellar ataxia type 35's Disease Ontology ID is recorded as DOID:0050982^[8].
• spinocerebellar ataxia type 35's Orphanet ID is recorded as 276193^[9].
• spinocerebellar ataxia type 35's genetic association is recorded as TGM6^[10].
• spinocerebellar ataxia type 35's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050982^[11].
• spinocerebellar ataxia type 35's exact match is recorded as http://identifiers.org/doid/DOID:0050982^[12].
• spinocerebellar ataxia type 35's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276193^[13].
• spinocerebellar ataxia type 35's UMLS CUI is recorded as C3888031^[14].
• spinocerebellar ataxia type 35's UMLS CUI is recorded as C1539956^[15].
• spinocerebellar ataxia type 35's ICD-10-CM is recorded as G11.8^[16].
• spinocerebellar ataxia type 35's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• spinocerebellar ataxia type 35's Mondo ID is recorded as MONDO_0013485^[18].
• spinocerebellar ataxia type 35's UniProt disease ID is recorded as DI-03054^[19].