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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: Jaundice (D007565)
..Starting node ..Jaundice, Obstructive (D041781)
Child Nodes:
........Anemia, hereditary spherocytic hemolytic (C536356)
........Jaundice, Familial Obstructive, of Infancy (C564118)
Sister Nodes:
..Deal Barratt Dillon syndrome (C538206)
..Dysmyelination With Jaundice (C565610)
..Jaundice, Obstructive (D041781) 2
..Lutz Richner Landolt syndrome (C537726)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5948
Name:	Jaundice, Obstructive
Definition:	Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS.
Alternative IDs:
ParentIDs:	MESH:D007565
TreeNumbers:	C23.550.429.500.755 \|C23.888.885.375.500
Synonyms:	Cholestatic Jaundice \|Jaundice, Cholestatic \|Jaundice, Mechanical \|Mechanical Jaundice \|Obstructive Jaundice
Slim Mappings:	Pathology (process)\|Signs and symptoms
Reference:	MedGen: D041781 MeSH: D041781 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants