Aplasia/Hypoplasia of the cerebellum

Symptom Information:

Symptom ID: HPO:0007360
Synonyms:
Atrophy/Degeneration affecting the cerebellum [HPO:0007360]
Atrophy/Hypoplasia of the cerebellum [HPO:0007360]
Cerebellar hypoplasia/atrophy [HPO:0007360]
Cerebellum vermis agenesis [Orphanet:42810]
Cerebellum/cerebellar vermis anomaly/agenesis/hypoplasia [Orphanet:42810]
Cerebellar hypoplasia and atrophy [OMIM:Cerebellar hypoplasia and atrophy]
Cerebellar hypoplasia/atrophy (27%) [OMIM:Cerebellar hypoplasia/atrophy (27%)]
Quality:
Cross references:
HPO:0006817 "Aplasia/Hypoplasia of the cerebellar vermis" [Orphanet:42810]
HPO:0001320 "Cerebellar vermis hypoplasia" [Orphanet:42810]
HPO:0002335 "Agenesis of cerebellar vermis" [Orphanet:42810]
Orphanet:42810 "Cerebellum/cerebellar vermis anomaly/agenesis/hypoplasia" [Orphanet:42810]
OMIM: "Cerebellar hypoplasia and atrophy" [OMIM:Cerebellar hypoplasia and atrophy]
OMIM: "Cerebellar hypoplasia/atrophy (27%)" [OMIM:Cerebellar hypoplasia/atrophy (27%)]
Is a (Direct Parents):
Orphanet Cerebellar vermis hypoplasia
HPO         Abnormality of the cerebellum
HPO         Aplasia/Hypoplasia involving the central nervous system
Orphanet Structural anomalies of the nervous system
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
Alström syndrome (Orphanet:64)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Bifunctional enzyme deficiency (Orphanet:300)
Constitutional megaloblastic anemia with severe neurologic disease (Orphanet:319651)
MELAS (Orphanet:550)
Maternally-inherited diabetes and deafness (Orphanet:225)
Mowat-Wilson syndrome (Orphanet:2152)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)