Disease #05429 (SCAR21 (ataxia, spinocerebellar, autosomal recrecessive, type 21 (SCAR-21)), OMIM:616719)
Official abbreviation |
SCAR21 |
Name |
ataxia, spinocerebellar, autosomal recrecessive, type 21 (SCAR-21) |
OMIM ID |
616719 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SCYL1 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2018-05-20 10:46:55 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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