Apathy

Symptom Information:

Symptom ID: HPO:0000741
Synonyms:
On examination - apathetic (finding) [Orphanet:43620]
Indifference (finding) [Orphanet:43620]
On examination - apathetic [Orphanet:43620]
Indifferent mood [Orphanet:43620]
Apathy [OMIM:Apathy]
Humour troubles/anxiety/depression/apathy/euphoria/irritability [Orphanet:43620]
Indifference [Orphanet:43620]
Apathy [Orphanet:43620]
Listless [Orphanet:43620]
Indifference [MedDRA:10021703]
Aloof [MedDRA:10021703]
Detached [MedDRA:10021703]
Indifference to circumstance [MedDRA:10021703]
Indifferent face [MedDRA:10021703]
La belle indifference [MedDRA:10021703]
Apathy [MedDRA:10002942]
Ambition loss of [MedDRA:10002942]
Initiative loss of [MedDRA:10002942]
Lack of motivation [MedDRA:10002942]
Loss of ambition [MedDRA:10002942]
Loss of initiative [MedDRA:10002942]
Avolition [MedDRA:10002942]
Listless [MedDRA:10024642]
Listlessness [MedDRA:10024642]
Indifference [OMIM:Indifference]
Euphoria [Orphanet:43620]
Euphoria [OMIM:Euphoria]
Quality:
Cross references:
Orphanet:43620 "Humour troubles/anxiety/depression/apathy/euphoria/irritability" [Orphanet:43620]
OMIM: "Apathy" [OMIM:Apathy]
OMIM: "Indifference" [OMIM:Indifference]
OMIM: "Euphoria" [OMIM:Euphoria]
UMLS:C0085632 "Apathy" [HPO:0000741]
UMLS:C0436596 "On examination - apathetic" [Orphanet:43620]
UMLS:C0085632 "Indifferent mood" [Orphanet:43620]
Is a (Direct Parents):
MedDRA Behaviour and socialisation disturbances
HPO         Diminished motivation
MedDRA Mood disorders NEC
Orphanet Behavioral abnormality
Orphanet Depression
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:
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)