Disease #03921 (SCAR14 (ataxia, spinocerebellar, autosomal recessive, type 14 (SCAR-14)), OMIM:615386)

Official abbreviation SCAR14
Name ataxia, spinocerebellar, autosomal recessive, type 14 (SCAR-14)
OMIM ID 615386
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SPTBN2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00025013 - - - - no United States white - - - - SCAR14 severe bulbar, cerebellar, and proprioceptive dysfunction - SPTBN2 2 1 Vikki Stefans
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