Disease #04529 (SCA15 (ataxia, spinocerebellar, type 15 (SCA-15)), OMIM:606658)

Official abbreviation SCA15
Name ataxia, spinocerebellar, type 15 (SCA-15)
OMIM ID 606658
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 ITPR1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00375524 180536 - - - - - Arabian - - - - SCA15 Dysarthria, Motor delay, Neurological speech impairment, Neurodevelopmental delay ITPR1 ITPR1 1 1 Andreas Laner
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