Aplasia/Hypoplasia of the cerebellar vermis

Symptom Information:

Symptom ID: HPO:0006817
Synonyms:
CEREBELLAR VERMIS APLASIA OR HYPOPLASIA [HPO:0006817]
Cerebellar vermis aplasia/hypoplasia [HPO:0006817]
Hypo/aplastic vermis [HPO:0006817]
Cerebellum vermis agenesis [Orphanet:42810]
Cerebellar vermis aplasia or hypoplasia [OMIM:Cerebellar vermis aplasia or hypoplasia]
Cerebellar vermis aplasia/hypoplasia [OMIM:Cerebellar vermis aplasia/hypoplasia]
Cerebellum/cerebellar vermis anomaly/agenesis/hypoplasia [Orphanet:42810]
Cerebellar vermis aplasia/ hypoplasia [OMIM:Cerebellar vermis aplasia/ hypoplasia]
Quality:
Cross references:
HPO:0001320 "Cerebellar vermis hypoplasia" [Orphanet:42810]
HPO:0002335 "Agenesis of cerebellar vermis" [Orphanet:42810]
HPO:0007360 "Aplasia/Hypoplasia of the cerebellum" [Orphanet:42810]
Orphanet:42810 "Cerebellum/cerebellar vermis anomaly/agenesis/hypoplasia" [Orphanet:42810]
OMIM: "Cerebellar vermis aplasia or hypoplasia" [OMIM:Cerebellar vermis aplasia or hypoplasia]
OMIM: "Cerebellar vermis aplasia/hypoplasia" [OMIM:Cerebellar vermis aplasia/hypoplasia]
OMIM: "Cerebellar vermis aplasia/ hypoplasia" [OMIM:Cerebellar vermis aplasia/ hypoplasia]
Is a (Direct Parents):
Orphanet Structural anomalies of the nervous system
Orphanet Cerebellar vermis hypoplasia
HPO         Abnormality of the cerebellar vermis
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
3C syndrome (Orphanet:7)
ARIMA SYNDROME (OMIM:243910)
Alström syndrome (Orphanet:64)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Christianson syndrome (Orphanet:85278)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome 5 (OMIM:610188)
Joubert syndrome with oculorenal defect (Orphanet:2318)
MELAS (Orphanet:550)
Maternally-inherited diabetes and deafness (Orphanet:225)
Mowat-Wilson syndrome (Orphanet:2152)
Opitz G/BBB syndrome (Orphanet:2745)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)