Abnormality of the cerebellum
Symptom Information:
Symptom ID:
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HPO:0001317
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Synonyms:
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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)] |
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Quality:
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Cross references:
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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)] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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36 / 7739
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Resource:
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All diseases associated with this symptom: