Pontocerebellar atrophy

Symptom Information:

Symptom ID: HPO:0006879
Synonyms:
Pontocerebellar atrophy [OMIM:Pontocerebellar atrophy]
Quality:
Cross references:
OMIM: "Pontocerebellar atrophy" [OMIM:Pontocerebellar atrophy]
Is a (Direct Parents):
HPO         Cerebellar atrophy
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

DPM1-CDG (Orphanet:79322)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
SPINOCEREBELLAR ATAXIA 40 (OMIM:616053)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Wolfram syndrome 1 (OMIM:222300)