Agitation
Symptom Information:
| Symptom ID: | HPO:0000713 | ||||
| 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) Agitation(HPO:0000713) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Agitation(HPO:0000713) |
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| Database Frequency: | 18 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
| Adenylosuccinate lyase deficiency | (Orphanet:46) |
| Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
| CLUSTER HEADACHE, FAMILIAL | (OMIM:119915) |
| Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
| FRAXE intellectual deficit | (Orphanet:100973) |
| Familial or sporadic hemiplegic migraine | (Orphanet:569) |
| Growth delay due to insulin-like growth factor I resistance | (Orphanet:73273) |
| Huntington disease | (Orphanet:399) |
| Isolated sulfite oxidase deficiency | (Orphanet:99731) |
| MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 | (OMIM:616116) |
| MENTAL RETARDATION, X-LINKED 30 | (OMIM:300558) |
| PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 | (OMIM:610489) |
| PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 | (OMIM:610475) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Primary pigmented nodular adrenocortical disease | (Orphanet:189439) |
| Progressive non-fluent aphasia | (Orphanet:100070) |
| X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome | (Orphanet:85295) |