Cerebellar dysplasia

Symptom Information:

Symptom ID: HPO:0007033
Synonyms:
Cerebellar dysplasia [OMIM:Cerebellar dysplasia]
Cerebellar dysplasia [MedDRA:10072942]
Quality:
Cross references:
OMIM: "Cerebellar dysplasia" [OMIM:Cerebellar dysplasia]
Is a (Direct Parents):
HPO         Abnormality of the cerebellum
MedDRA Congenital cerebellar disorders
Is a (Whole tree): HPO:
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Congenital and peripartum neurological conditions(MedDRA:10010335)
       Congenital cerebellar disorders(MedDRA:10010413)
          Cerebellar dysplasia(HPO:0007033)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
Cataract - nephropathy - encephalopathy (Orphanet:1380)
Chudley-McCullough syndrome (Orphanet:314597)
Joubert syndrome 21 (OMIM:615636)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10 (OMIM:615041)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 (OMIM:615181)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 (OMIM:613153)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
Muscle-eye-brain disease (Orphanet:588)
PORETTI-BOLTSHAUSER SYNDROME (OMIM:615960)