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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: Lupus Erythematosus, Systemic (D008180)
Parent Node: Nephritis (D009393)
..Starting node ..SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2 (OMIM:607966)
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:	10843
Name:	SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2
Definition:
Alternative IDs:
ParentIDs:	MESH:D008180\|MESH:D009393
TreeNumbers:	C12.777.419.570/607966 \|C13.351.968.419.570/607966 \|C17.300.480/607966 \|C20.111.590/607966
Synonyms:	SLEN2
Slim Mappings:	Connective tissue disease\|Immune system disease\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: 607966 MeSH: 607966 OMIM: 607966; Genes:
Phenotypes
Disease Causing ClinVar Variants