SPINOCEREBELLAR ATAXIA 37

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 615945
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0000639) Nystagmus rare [HPO:skoehler] 555 / 7739
2
 (HPO:0001337) Tremor rare [HPO:skoehler] 200 / 7739
3
 (HPO:0002317) Unsteady gait 45 / 7739
4
 (HPO:0001251) Ataxia 413 / 7739
5
 (HPO:0002015) Dysphagia rare [HPO:skoehler] 301 / 7739
6
 (HPO:0001260) Dysarthria 329 / 7739
7
 (HPO:0002359) Frequent falls 24 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: