SPINOCEREBELLAR ATAXIA 38

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 615957
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 555 / 7739
2
 (HPO:0000514) Slow saccadic eye movements 21 / 7739
3
 (HPO:0003477) Peripheral axonal neuropathy rare [HPO:skoehler] 62 / 7739
4
 (HPO:0002070) Limb ataxia 41 / 7739
5
 (HPO:0001260) Dysarthria 329 / 7739
6
 (HPO:0002066) Gait ataxia 327 / 7739
7
 (HPO:0001272) Cerebellar atrophy 197 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: