Restlessness
Symptom Information:
| Symptom ID: | HPO:0000711 | ||||
| Synonyms: |
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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 higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Abnormal emotion/affect behavior(HPO:0100851) Restlessness(HPO:0000711) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Restlessness(HPO:0000711) |
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| Database Frequency: | 18 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
| CLUSTER HEADACHE, FAMILIAL | (OMIM:119915) |
| Citrullinemia type I | (Orphanet:247525) |
| Citrullinemia type II | (Orphanet:247585) |
| Glycine encephalopathy | (Orphanet:407) |
| Huntington disease-like 1 | (Orphanet:157941) |
| Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
| MENTAL RETARDATION, X-LINKED 30 | (OMIM:300558) |
| Marden-Walker syndrome | (Orphanet:2461) |
| McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
| Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
| Pontocerebellar hypoplasia type 2 | (Orphanet:2524) |
| Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |
| Progressive non-fluent aphasia | (Orphanet:100070) |
| Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
| Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:35123) |
| Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
| X-linked spastic paraplegia type 16 | (Orphanet:100997) |