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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: Hyperbilirubinemia (D006932)
Parent Node: Skin Manifestations (D012877)
..Starting node ..Jaundice (D007565)
Child Nodes:
........Deal Barratt Dillon syndrome (C538206)
........Dysmyelination With Jaundice (C565610)
........Jaundice, Obstructive (D041781) 2
........Lutz Richner Landolt syndrome (C537726)
Sister Nodes:
..Cafe-au-Lait Spots (D019080) 4
..Ecchymosis (D004438)
..Jaundice (D007565) 6
..Livedo Reticularis (D054068) 1
..Necrolytic Migratory Erythema (D058568)
..Pallor (D010167)
..Pruritus (D011537) 6
..Purpura (D011693) 15
..Striae Distensae (D057896) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5944
Name:	Jaundice
Definition:	A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction.
Alternative IDs:
ParentIDs:	MESH:D006932\|MESH:D012877
TreeNumbers:	C23.550.429.500 \|C23.888.885.375
Synonyms:	Hemolytic Jaundice \|Hemolytic Jaundices \|Icterus \|Jaundice, Hemolytic \|Jaundices, Hemolytic
Slim Mappings:	Pathology (process)\|Signs and symptoms
Reference:	MedGen: D007565 MeSH: D007565 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants