Disease #06425 (SCAR26 (?Spinocerebellar ataxia, autosomal recessive 26), OMIM:617633)

Official abbreviation SCAR26
Name ?Spinocerebellar ataxia, autosomal recessive 26
OMIM ID 617633
Human Phenotype Ontology Project (HPO) HPO
Inheritance Digenic
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene XRCC1
Associated tissues -
Disease features onset adulthood, cerebellar ataxia (HP:0001251), cerebellar atrophy (HP:0001272), peripheral neuropathy (HP:0009830), distal muscle weakness (HP:0002460), no developmental delay (-HP:0001263), no seizures (-HP:0001250), hyporeflexia (HP:0001265), no cognitive impairment (-HP:0100543), oculomotor apraxia (HP:0000657),no dystonia (-HP:0001332)
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-09-10 20:59:56 +02:00 (CEST)

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