spinocerebellar ataxia type 34
Human disease
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spinocerebellar ataxia type 34
Summary
spinocerebellar ataxia type 34 is a developmental defect during embryogenesis[1].
Key Facts
- spinocerebellar ataxia type 34's instance of is recorded as developmental defect during embryogenesis[2].
- spinocerebellar ataxia type 34's instance of is recorded as rare disease[3].
- spinocerebellar ataxia type 34's instance of is recorded as class of disease[4].
- spinocerebellar ataxia type 34 is a type of Erythrokeratodermia[5].
- spinocerebellar ataxia type 34 is a type of spinocerebellar ataxia[6].
- spinocerebellar ataxia type 34 is a type of autosomal dominant cerebellar ataxia type I[7].
- spinocerebellar ataxia type 34 is a type of genetic epidermal disorder[8].
- spinocerebellar ataxia type 34's health specialty is recorded as medical genetics[9].
- spinocerebellar ataxia type 34's genetic association is recorded as ELOVL4[10].
- spinocerebellar ataxia type 34's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050981[11].
- spinocerebellar ataxia type 34's exact match is recorded as http://identifiers.org/doid/DOID:0050981[12].
- spinocerebellar ataxia type 34's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1955[13].
- spinocerebellar ataxia type 34's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].