Abnormality of the cerebellum

Symptom Information:

Symptom ID: HPO:0001317
Synonyms:
Cerebellar abnormalities [HPO:0001317]
Cerebellar abnormality [HPO:0001317]
Cerebellar anomaly [HPO:0001317]
Cerebellar signs [HPO:0001317]
Cerebellar abnormalities [OMIM:Cerebellar abnormalities]
Cerebellar anomaly [OMIM:Cerebellar anomaly]
Cerebellar signs [OMIM:Cerebellar signs]
Cerebellar anomalies [OMIM:Cerebellar anomalies]
Cerebellar signs (in some patients) [OMIM:Cerebellar signs (in some patients)]
Cerebellar signs (less common) [OMIM:Cerebellar signs (less common)]
Cerebellar signs (may be permanent in 50% of patients) [OMIM:Cerebellar signs (may be permanent in 50% of patients)]
Cerebellar signs (more common in variant CJD) [OMIM:Cerebellar signs (more common in variant CJD)]
Quality:
Cross references:
OMIM: "Cerebellar abnormalities" [OMIM:Cerebellar abnormalities]
OMIM: "Cerebellar anomaly" [OMIM:Cerebellar anomaly]
OMIM: "Cerebellar signs" [OMIM:Cerebellar signs]
OMIM: "Cerebellar anomalies" [OMIM:Cerebellar anomalies]
OMIM: "Cerebellar signs (in some patients)" [OMIM:Cerebellar signs (in some patients)]
OMIM: "Cerebellar signs (less common)" [OMIM:Cerebellar signs (less common)]
OMIM: "Cerebellar signs (may be permanent in 50% of patients)" [OMIM:Cerebellar signs (may be permanent in 50% of patients)]
OMIM: "Cerebellar signs (more common in variant CJD)" [OMIM:Cerebellar signs (more common in variant CJD)]
Is a (Direct Parents):
HPO         Abnormality of the metencephalon
HPO         Cerebellar gliosis
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

4q21 microdeletion syndrome (Orphanet:238750)
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Autosomal recessive spastic paraplegia type 21 (Orphanet:101001)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
Autosomal recessive spastic paraplegia type 5A (Orphanet:100986)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 (OMIM:602197)
CLN13 disease (Orphanet:352709)
CLN3 disease (Orphanet:228346)
CLN4B disease (Orphanet:228343)
Creutzfeldt-Jakob disease (Orphanet:204)
EPILEPSY, PROGRESSIVE MYOCLONIC, 5 (OMIM:613832)
Giant axonal neuropathy (Orphanet:643)
Griscelli disease type 2 (Orphanet:79477)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hypomyelination - congenital cataract (Orphanet:85163)
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia (Orphanet:284332)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
MELAS (Orphanet:550)
MIGRAINE, FAMILIAL HEMIPLEGIC, 1 (OMIM:141500)
Neuroferritinopathy (Orphanet:157846)
Odontoleukodystrophy (Orphanet:77295)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Spastic paraplegia type 2 (Orphanet:99015)
Tremor - nystagmus - duodenal ulcer (Orphanet:3350)
Wolfram syndrome 1 (OMIM:222300)
X-linked intellectual deficit - cerebellar hypoplasia (Orphanet:137831)