Apathy
Symptom Information:
Symptom ID: | HPO:0000741 | |||||||||||||||||||||||||||
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) Abnormal emotion/affect behavior(HPO:0100851) Diminished motivation(HPO:0000745) Apathy(HPO:0000741) MedDRA: |
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Database Frequency: | 42 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:612069) |
Aceruloplasminemia | (Orphanet:48818) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 | (OMIM:615483) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
CACH syndrome | (Orphanet:135) |
CADASIL | (Orphanet:136) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Classical phenylketonuria | (Orphanet:79254) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Congenital or early infantile CACH syndrome | (Orphanet:157713) |
Cree leukoencephalopathy | (Orphanet:99854) |
Creutzfeldt-Jakob disease | (Orphanet:204) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
FRONTOTEMPORAL DEMENTIA | (OMIM:600274) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105550) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Fetal Gaucher disease | (Orphanet:85212) |
Frontotemporal dementia | (Orphanet:282) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
GM2-gangliosidosis, AB variant | (Orphanet:309246) |
Huntington disease | (Orphanet:399) |
Huntington disease-like 2 | (Orphanet:98934) |
Inherited Creutzfeldt-Jakob disease | (Orphanet:282166) |
Juvenile or adult CACH syndrome | (Orphanet:157719) |
Kleefstra syndrome | (Orphanet:261494) |
Late infantile CACH syndrome | (Orphanet:157716) |
MELAS | (Orphanet:550) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
Nasu-Hakola disease | (Orphanet:2770) |
Nephronophthisis 1 | (OMIM:256100) |
Ovarioleukodystrophy | (Orphanet:99853) |
PICK DISEASE OF BRAIN | (OMIM:172700) |
Perry syndrome | (Orphanet:178509) |
Progressive non-fluent aphasia | (Orphanet:100070) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |
Tay-Sachs disease | (Orphanet:845) |