Cerebellar atrophy, severe

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Cerebellar atrophy, severe" [OMIM:Cerebellar atrophy, severe]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset autosomal recessive cerebellar ataxia (Orphanet:284289)