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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Neurobehavioral Manifestations (D019954)
..Starting node ..Anhedonia (D059445)
Child Nodes:
Sister Nodes:
..Anhedonia (D059445)
..Apraxias (D001072) 10
..Catatonia (D002389) 1
..Communication Disorders (D003147) 57
..Confusion (D003221) 2
..Consciousness Disorders (D003244) 11
..Intellectual Disability (D008607) 579
..Lethargy (D053609)
..Memory Disorders (D008569) 7
..Perceptual Disorders (D010468) 13
..Psychomotor Disorders (D011596) 34
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	702
Name:	Anhedonia
Definition:	Inability to experience pleasure due to impairment or dysfunction of normal psychological and neurobiological mechanisms. It is a symptom of many PSYCHOTIC DISORDERS (e.g., DEPRESSIVE DISORDER, MAJOR; and SCHIZOPHRENIA).
Alternative IDs:
ParentIDs:	MESH:D019954
TreeNumbers:	C10.597.606.057 \|C23.888.592.604.039
Synonyms:	Anhedonia, Physical \|Anhedonias \|Anhedonia, Social \|Anhedonias, Physical \|Anhedonias, Social \|Physical Anhedonia \|Physical Anhedonias \|Social Anhedonia \|Social Anhedonias
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D059445 MeSH: D059445 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants