Disease browser and phenotype portal

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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: Disease Attributes (D020969)
..Starting node ..Iatrogenic Disease (D007049)
Child Nodes:
Sister Nodes:
..Acute Disease (D000208)
..Asymptomatic Diseases (D058070) 1
..Catastrophic Illness (D002388)
..Chronic Disease (D002908)
..Convalescence (D003289)
..Critical Illness (D016638)
..Disease Progression (D018450) 1
..Disease Resistance (D060467)
..Disease Susceptibility (D004198) 11
..Diseases in Twins (D004200)
..Emergencies (D004630)
..Facies (D019066) 142
..Iatrogenic Disease (D007049)
..Neglected Diseases (D058069)
..Rare Diseases (D035583)
..Recurrence (D012008)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5664
Name:	Iatrogenic Disease
Definition:	Any adverse condition in a patient occurring as the result of treatment by a physician, surgeon, or other health professional, especially infections acquired by the patient during the course of treatment.
Alternative IDs:
ParentIDs:	MESH:D020969
TreeNumbers:	C23.550.291.875
Synonyms:	Disease, Iatrogenic \|Diseases, Iatrogenic \|Iatrogenic Diseases
Slim Mappings:	Pathology (process)
Reference:	MedGen: D007049 MeSH: D007049 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants