Disease #00216 (SCA35 (ataxia, spinocerebellar, type 35 (SCA-35)), OMIM:613908)
Official abbreviation |
SCA35 |
Name |
ataxia, spinocerebellar, type 35 (SCA-35) |
OMIM ID |
613908 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
TGM6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-10-02 11:35:03 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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