Intention tremor
Symptom Information:
Symptom ID: | HPO:0002080 | |||||
Synonyms: |
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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) Intention tremor(HPO:0002080) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Tremor(HPO:0001337) Intention tremor(HPO:0002080) |
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Database Frequency: | 44 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Adult-onset autosomal recessive cerebellar ataxia | (Orphanet:284289) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME1 | (OMIM:224050) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cerebellar ataxia, Cayman type | (Orphanet:94122) |
Cowden syndrome | (Orphanet:201) |
Dysequilibrium syndrome | (Orphanet:1766) |
EAST syndrome | (Orphanet:199343) |
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD | (OMIM:130950) |
EPISODIC ATAXIA, TYPE 8 | (OMIM:616055) |
Erythrokeratodermia - ataxia | (Orphanet:1955) |
Familial dementia, Danish type | (Orphanet:97346) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Gaucher disease type 3 | (Orphanet:77261) |
Glutathione synthetase deficiency with 5-oxoprolinuria | (Orphanet:289846) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia | (Orphanet:284332) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
LEUKODYSTROPHY, HYPOMYELINATING, 9 | (OMIM:616140) |
Leukoencephalopathy - dystonia - motor neuropathy | (Orphanet:163684) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
PEROXISOME BIOGENESIS DISORDER 6B | (OMIM:614871) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Proteus-like syndrome | (Orphanet:2969) |
Ramsay-Hunt syndrome | (Orphanet:3020) |
SPINOCEREBELLAR ATAXIA 40 | (OMIM:616053) |
Spectrin-associated autosomal recessive cerebellar ataxia | (Orphanet:352403) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 29 | (Orphanet:208513) |
Spinocerebellar ataxia type 35 | (Orphanet:276193) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |
TMCO1 defect syndrome | (Orphanet:228407) |
TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS | (OMIM:190200) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked progressive cerebellar ataxia | (Orphanet:1175) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |