Depression
Symptom Information:
Symptom ID: | HPO:0000716 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Depression(HPO:0000716) MedDRA: |
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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) |