Action tremor

Symptom Information:

Symptom ID: HPO:0002345
Synonyms:
Action tremor [OMIM:Action tremor]
Tremor, action [OMIM:Tremor, action]
Tremor, action (arms, tongue, head, legs and trunk) [OMIM:Tremor, action (arms, tongue, head, legs and trunk)]
Action tremor [MedDRA:10072413]
Quality:
Cross references:
OMIM: "Action tremor" [OMIM:Action tremor]
OMIM: "Tremor, action" [OMIM:Tremor, action]
OMIM: "Tremor, action (arms, tongue, head, legs and trunk)" [OMIM:Tremor, action (arms, tongue, head, legs and trunk)]
Is a (Direct Parents):
HPO         Kinetic tremor
HPO         Isometric tremor
HPO         Titubation
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)
                   Action tremor(HPO:0002345)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Tremor(HPO:0001337)
          Action tremor(HPO:0002345)
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)