Action tremor
Symptom Information:
Symptom ID: | HPO:0002345 | ||||||||||
Synonyms: |
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Quality: | |||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Tremor(HPO:0001337) Action tremor(HPO:0002345) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Tremor(HPO:0001337) Action tremor(HPO:0002345) |
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Database Frequency: | 11 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Huntington disease-like 2 | (Orphanet:98934) |
LICHTENSTEIN-KNORR SYNDROME | (OMIM:616291) |
Spinocerebellar ataxia type 12 | (Orphanet:98762) |
Spinocerebellar ataxia type 15/16 | (Orphanet:98769) |
Spinocerebellar ataxia type 20 | (Orphanet:101110) |
TREMOR, HEREDITARY ESSENTIAL, 1 | (OMIM:190300) |
TREMOR, HEREDITARY ESSENTIAL, 4 | (OMIM:614782) |
X-linked non progressive cerebellar ataxia | (Orphanet:314978) |
X-linked progressive cerebellar ataxia | (Orphanet:1175) |