Disease #07071 (SCA4 (ataxia, spinocerebellar, type 4), OMIM:600223)

Official abbreviation SCA4
Name ataxia, spinocerebellar, type 4
OMIM ID 600223
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ZFHX3
Associated tissues -
Disease features -
Remarks -
Date created 2024-03-06 19:58:38 +01:00 (CET)
Date last edited N/A

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