Personality changes
Symptom Information:
| Symptom ID: | HPO:0000751 | ||||
| Synonyms: |
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| Quality: | |||||
| Cross references: |
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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) Personality changes(HPO:0000751) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Personality changes(HPO:0000751) |
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| Database Frequency: | 33 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| ALZHEIMER DISEASE 10 | (OMIM:609636) |
| ALZHEIMER DISEASE 3 | (OMIM:607822) |
| Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
| Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
| Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
| CACH syndrome | (Orphanet:135) |
| CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY | (OMIM:607674) |
| Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
| Choreoacanthocytosis | (Orphanet:2388) |
| Congenital or early infantile CACH syndrome | (Orphanet:157713) |
| Cree leukoencephalopathy | (Orphanet:99854) |
| Creutzfeldt-Jakob disease | (Orphanet:204) |
| FRONTOTEMPORAL DEMENTIA | (OMIM:600274) |
| Fabry disease | (Orphanet:324) |
| Frontotemporal dementia | (Orphanet:282) |
| Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
| Huntington disease | (Orphanet:399) |
| Huntington disease-like 1 | (Orphanet:157941) |
| Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
| Juvenile Huntington disease | (Orphanet:248111) |
| Juvenile or adult CACH syndrome | (Orphanet:157719) |
| Late infantile CACH syndrome | (Orphanet:157716) |
| MELAS | (Orphanet:550) |
| McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
| Nasal dermoid cyst | (Orphanet:141103) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Ovarioleukodystrophy | (Orphanet:99853) |
| PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
| PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION | (OMIM:172500) |
| PICK DISEASE OF BRAIN | (OMIM:172700) |
| Progressive non-fluent aphasia | (Orphanet:100070) |
| SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES | (OMIM:606688) |
| Wilson disease | (Orphanet:905) |