Cerebellar vermis atrophy

Symptom Information:

Symptom ID: HPO:0006855
Synonyms:
Atrophy of cerebellar vermis [HPO:0006855]
Atrophy of the cerebellar vermis [HPO:0006855]
Atrophy of cerebellar vermis [OMIM:Atrophy of cerebellar vermis]
Cerebellar vermis atrophy [OMIM:Cerebellar vermis atrophy]
Quality:
Cross references:
OMIM: "Atrophy of cerebellar vermis" [OMIM:Atrophy of cerebellar vermis]
OMIM: "Cerebellar vermis atrophy" [OMIM:Cerebellar vermis atrophy]
Is a (Direct Parents):
HPO         Abnormality of the cerebellar vermis
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Adenylosuccinate lyase deficiency (Orphanet:46)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Behr syndrome (Orphanet:1239)
Familial paroxysmal ataxia (Orphanet:97)
Friedreich ataxia 2 (OMIM:601992)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 (OMIM:614255)
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY (OMIM:615760)
Spinocerebellar ataxia type 29 (Orphanet:208513)