Cerebellar atrophy, progressive

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Cerebellar atrophy, progressive (1 patient) [OMIM:Cerebellar atrophy, progressive (1 patient)]
Cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) [OMIM:Cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)]
Quality:
Cross references:
OMIM: "Cerebellar atrophy, progressive" [OMIM:Cerebellar atrophy, progressive]
OMIM: "Cerebellar atrophy, progressive (1 patient)" [OMIM:Cerebellar atrophy, progressive (1 patient)]
OMIM: "Cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)" [OMIM:Cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Infantile cerebellar-retinal degeneration (Orphanet:313850)
Myhre syndrome (Orphanet:2588)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D (OMIM:613811)
Progressive epilepsy-intellectual deficit, Finnish type (Orphanet:1947)