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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: Hypertension, Pregnancy-Induced (D046110)
..Starting node ..HELLP Syndrome (D017359)
Child Nodes:
Sister Nodes:
..Eclampsia (D004461)
..HELLP Syndrome (D017359)
..Pre-Eclampsia (D011225) 4
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4970
Name:	HELLP Syndrome
Definition:	A syndrome of HEMOLYSIS, elevated liver ENZYMES, and low blood platelets count (THROMBOCYTOPENIA). HELLP syndrome is observed in pregnant women with PRE-ECLAMPSIA or ECLAMPSIA who also exhibit LIVER damage and abnormalities in BLOOD COAGULATION.
Alternative IDs:
ParentIDs:	MESH:D046110
TreeNumbers:	C13.703.395.186
Synonyms:	Hemolysis, Elevated Liver Enzymes, Lowered Platelets \|Syndrome, HELLP
Slim Mappings:	Pregnancy complication
Reference:	MedGen: D017359 MeSH: D017359 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants