Cerebellar atrophy, mild

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Cerebellar atrophy, mild (1 patient) [OMIM:Cerebellar atrophy, mild (1 patient)]
Cerebellar atrophy, mild (in 1 of 3 families) [OMIM:Cerebellar atrophy, mild (in 1 of 3 families)]
Quality:
Cross references:
OMIM: "Cerebellar atrophy, mild" [OMIM:Cerebellar atrophy, mild]
OMIM: "Cerebellar atrophy, mild (1 patient)" [OMIM:Cerebellar atrophy, mild (1 patient)]
OMIM: "Cerebellar atrophy, mild (in 1 of 3 families)" [OMIM:Cerebellar atrophy, mild (in 1 of 3 families)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic paraplegia type 30 (Orphanet:101010)
Bilateral generalized polymicrogyria (Orphanet:208447)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
Spinocerebellar ataxia type 3 (Orphanet:98757)