Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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, Renal (D006977)
Parent Node: Nephritis (D009393)
..Starting node ..Hypertensive Nephropathy (C563161)
Child Nodes:
Sister Nodes:
..Dyschondrosteosis and Nephritis (C565080)
..Glomerulonephritis (D005921) 21
..Hypertensive Nephropathy (C563161)
..Nephritis, Hereditary (D009394) 11
..Nephritis, Interstitial (D009395) 8
..Pyelitis (D011702) 3
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1 (OMIM:607965)
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2 (OMIM:607966)
..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3 (OMIM:607967)
..Yorifuji Okuno syndrome (C536714)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5498
Name:	Hypertensive Nephropathy
Definition:
Alternative IDs:	OMIM:608026
ParentIDs:	MESH:D006977\|MESH:D009393
TreeNumbers:	C12.777.419.331/C563161 \|C12.777.419.570/C563161 \|C13.351.968.419.331/C563161 \|C13.351.968.419.570/C563161 \|C14.907.489.631/C563161
Synonyms:	HNP1
Slim Mappings:	Cardiovascular disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C563161 MeSH: C563161 OMIM: 608026; Genes:
Phenotypes
Disease Causing ClinVar Variants