Postural tremor

Symptom Information:

Symptom ID: HPO:0002174
Synonyms:
TREMOR, POSTURAL [HPO:0002174]
Postural tremor [OMIM:Postural tremor]
Tremor, postural [OMIM:Tremor, postural]
Postural tremor (later onset, spreads to all limbs and neck) [OMIM:Postural tremor (later onset, spreads to all limbs and neck)]
Tremor, postural (arms, tongue, head, legs and trunk) [OMIM:Tremor, postural (arms, tongue, head, legs and trunk)]
Postural tremor [MedDRA:10073211]
Quality:
Cross references:
OMIM: "Postural tremor" [OMIM:Postural tremor]
OMIM: "Tremor, postural" [OMIM:Tremor, postural]
OMIM: "Postural tremor (later onset, spreads to all limbs and neck)" [OMIM:Postural tremor (later onset, spreads to all limbs and neck)]
OMIM: "Tremor, postural (arms, tongue, head, legs and trunk)" [OMIM:Tremor, postural (arms, tongue, head, legs and trunk)]
Is a (Direct Parents):
HPO         Tremor
MedDRA 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)
                   Postural tremor(HPO:0002174)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Tremor(HPO:0001337)
          Postural tremor(HPO:0002174)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 8 (OMIM:608627)
Action myoclonus - renal failure syndrome (Orphanet:163696)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION (OMIM:300619)
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (Orphanet:284324)
Dystonia 16 (Orphanet:210571)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Leber hereditary optic neuropathy (Orphanet:104)
Leber plus disease (Orphanet:99718)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
Odontoleukodystrophy (Orphanet:77295)
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:606324)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Spinocerebellar ataxia type 15/16 (Orphanet:98769)
Spinocerebellar ataxia type 19/22 (Orphanet:98772)
Spinocerebellar ataxia type 2 (Orphanet:98756)
Spinocerebellar ataxia type 20 (Orphanet:101110)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Spinocerebellar ataxia type 27 (Orphanet:98764)
TREMOR, HEREDITARY ESSENTIAL, 1 (OMIM:190300)
TREMOR, HEREDITARY ESSENTIAL, 4 (OMIM:614782)
[DEL] LEBER OPTIC ATROPHY (OMIM:535000)