Disease #06705 (SCAR25 (?Spinocerebellar ataxia, autosomal recessive 25), OMIM:617584)

Official abbreviation SCAR25
Name ?Spinocerebellar ataxia, autosomal recessive 25
OMIM ID 617584
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ATG5
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.