Disease #04243 (SCAR17 (ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17)), OMIM:616127)
Official abbreviation |
SCAR17 |
Name |
ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17) |
OMIM ID |
616127 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
CWF19L1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-05-01 15:29:36 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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