Depression

Symptom Information:

Symptom ID: HPO:0000716
Synonyms:
Depressive disorder [HPO:0000716]
Depressed mood (finding) [Orphanet:43620]
Depressive disorder (disorder) [Orphanet:43620]
Depressed [HPO:0000716]
Depressive disorder [Orphanet:43620]
Mental Depression [Orphanet:43620]
Depressive episode, unspecified [Orphanet:43620]
Depressed mood [Orphanet:43620]
Depression [OMIM:Depression]
Humour troubles/anxiety/depression/apathy/euphoria/irritability [Orphanet:43620]
Depressive illness [Orphanet:43620]
Depressive episode [Orphanet:43620]
Depressive neurosis [Orphanet:43620]
Depression [Orphanet:43620]
Depressed mood [MedDRA:10012374]
Chronic depressive mood [MedDRA:10012374]
Dejection emotional [MedDRA:10012374]
Emotional dejection [MedDRA:10012374]
Feeling blue [MedDRA:10012374]
Feeling down [MedDRA:10012374]
Feeling sad [MedDRA:10012374]
Low mood [MedDRA:10012374]
Mood depression [MedDRA:10012374]
Mood depressions [MedDRA:10012374]
Sinking feeling [MedDRA:10012374]
Unhappiness [MedDRA:10012374]
Depression [MedDRA:10012378]
Anxiety depression [MedDRA:10012378]
Anxiety/depression [MedDRA:10012378]
Anxious depression [MedDRA:10012378]
Atypical depressive disorder [MedDRA:10012378]
Brief depressive reaction [MedDRA:10012378]
Depressed reaction [MedDRA:10012378]
Depressed state [MedDRA:10012378]
Depression aggravated [MedDRA:10012378]
Depression functional [MedDRA:10012378]
Depression mental [MedDRA:10012378]
Depression NOS [MedDRA:10012378]
Depression psychic [MedDRA:10012378]
Depression reactive [MedDRA:10012378]
Depression worsened [MedDRA:10012378]
Depressive disorder [MedDRA:10012378]
Depressive disorder, not elsewhere classified [MedDRA:10012378]
Depressive episode [MedDRA:10012378]
Depressive illness [MedDRA:10012378]
Depressive reaction [MedDRA:10012378]
Depressive stupor [MedDRA:10012378]
Exogenous depression [MedDRA:10012378]
Mixed anxiety &
depressive [MedDRA:10012378]
Reactive depression [MedDRA:10012378]
Unipolar depression [MedDRA:10012378]
Unipolar depressive illness [MedDRA:10012378]
Depressive state [MedDRA:10012378]
Acute depression [MedDRA:10012378]
Chronic depression [MedDRA:10012378]
Recurrent depressive disorder [MedDRA:10012378]
Anxiodepressive syndrome [MedDRA:10012378]
Dysthymic disorder [MedDRA:10013982]
Chronic depressive personality disorder [MedDRA:10013982]
Depression neurotic [MedDRA:10013982]
Depressive neurosis [MedDRA:10013982]
Depressive personality disorder [MedDRA:10013982]
Dysthymia [MedDRA:10013982]
Neurotic depression [MedDRA:10013982]
Depression (1 patient) [OMIM:Depression (1 patient)]
Depression (HCP) [OMIM:Depression (HCP)]
Depression (in some patients) [OMIM:Depression (in some patients)]
Euphoria [Orphanet:43620]
Euphoria [OMIM:Euphoria]
Depressive disorders [MedDRA:10012401]
Quality:
Cross references:
Orphanet:43620 "Humour troubles/anxiety/depression/apathy/euphoria/irritability" [Orphanet:43620]
OMIM: "Depression" [OMIM:Depression]
OMIM: "Depression (1 patient)" [OMIM:Depression (1 patient)]
OMIM: "Depression (HCP)" [OMIM:Depression (HCP)]
OMIM: "Depression (in some patients)" [OMIM:Depression (in some patients)]
OMIM: "Euphoria" [OMIM:Euphoria]
UMLS:C0344315 "Depressed" [HPO:0000716]
UMLS:C0011581 "Depressive disorder" [Orphanet:43620]
UMLS:C0011570 "Mental Depression" [Orphanet:43620]
UMLS:C0349217 "Depressive episode, unspecified" [Orphanet:43620]
UMLS:C0344315 "Depressed mood" [Orphanet:43620]
Is a (Direct Parents):
HPO         Abnormal emotion/affect behavior
MedDRA Mood alterations with depressive symptoms
Orphanet Behavioral abnormality
MedDRA Depressed mood disorders and disturbances
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)
                      Depression(HPO:0000716)
MedDRA:
Database Frequency: 99 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1 (OMIM:604348)
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY (OMIM:614307)
Aceruloplasminemia (Orphanet:48818)
Acute intermittent porphyria (Orphanet:79276)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Adult-onset dystonia-parkinsonism (Orphanet:199351)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Alström syndrome (Orphanet:64)
Argininemia (Orphanet:90)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 (OMIM:615007)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CADASIL (Orphanet:136)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CLN1 disease (Orphanet:228329)
CLN13 disease (Orphanet:352709)
CLN4A disease (Orphanet:228340)
CLN4B disease (Orphanet:228343)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cerebellar ataxia-deafness-narcolepsy syndrome (Orphanet:314404)
Citrullinemia type II (Orphanet:247585)
Classical homocystinuria (Orphanet:394)
Classical phenylketonuria (Orphanet:79254)
Creutzfeldt-Jakob disease (Orphanet:204)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT (OMIM:128100)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 2 (OMIM:603204)
EPILEPSY, NOCTURNAL FRONTAL LOBE, 5 (OMIM:615005)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105550)
Fabry disease (Orphanet:324)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Frontotemporal dementia with motor neuron disease (Orphanet:275872)
Gaucher disease type 3 (Orphanet:77261)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hemochromatosis, type 1 (OMIM:235200)
Hereditary coproporphyria (Orphanet:79273)
Huntington disease (Orphanet:399)
Huntington disease-like 1 (Orphanet:157941)
Huntington disease-like 2 (Orphanet:98934)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Juvenile Huntington disease (Orphanet:248111)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
MAJOR AFFECTIVE DISORDER 1 (OMIM:125480)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO (OMIM:126200)
Maternal hyperphenylalaninemia (Orphanet:2209)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Myoclonus-dystonia syndrome (Orphanet:36899)
NARP syndrome (Orphanet:644)
Nasu-Hakola disease (Orphanet:2770)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION (OMIM:172500)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 (OMIM:613077)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Perry syndrome (Orphanet:178509)
Phenylketonuria (Orphanet:716)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Recessive mitochondrial ataxia syndrome (Orphanet:94125)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Sneddon syndrome (Orphanet:820)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 14 (Orphanet:98763)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 27 (Orphanet:98764)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)
Stiff person syndrome (Orphanet:3198)
TRIMETHYLAMINURIA (OMIM:602079)
Wilson disease (Orphanet:905)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome 2 (OMIM:604928)
Wolfram-like syndrome (ORPHA:411590)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)