Disease #06030 (SCA47 (Spinocerebellar ataxia 47), OMIM:617931)

Official abbreviation SCA47
Name Spinocerebellar ataxia 47
OMIM ID 617931
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PUM1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00433150 251598 - - F ? ? (unknown) - - - - - SCA47 Neurodevelopmental abnormality, Intellectual disability, Bilateral tonic-clonic seizure, Seizure PUM1 PUM1 1 1 Andreas Laner
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