Intention tremor

Symptom Information:

Symptom ID: HPO:0002080
Synonyms:
Intention tremor [OMIM:Intention tremor]
Intention tremor (55%) [OMIM:Intention tremor (55%)]
Intention tremor (in some) [OMIM:Intention tremor (in some)]
Tremor, intention [OMIM:Tremor, intention]
Intention tremor [MedDRA:10022520]
Quality:
Cross references:
OMIM: "Intention tremor" [OMIM:Intention tremor]
OMIM: "Intention tremor (55%)" [OMIM:Intention tremor (55%)]
OMIM: "Intention tremor (in some)" [OMIM:Intention tremor (in some)]
OMIM: "Tremor, intention" [OMIM:Tremor, intention]
Is a (Direct Parents):
MedDRA Tremor
HPO         Tremor
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)
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)