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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: Genetic Diseases, X-Linked (D040181)
Parent Node: Vesico-Ureteral Reflux (D014718)
..Starting node ..Vesicoureteral Reflux, X-Linked (C564042)
Child Nodes:
Sister Nodes:
..Cakut (C566906)
..Papillorenal syndrome (C537168)
..Vesicoureteral Reflux 2 (C567053)
..VESICOURETERAL REFLUX 3 (OMIM:613674)
..Vesicoureteral Reflux, X-Linked (C564042)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

11595

Name:

Vesicoureteral Reflux, X-Linked

Definition:

Alternative IDs:

ParentIDs:

MESH:D014718|MESH:D040181

TreeNumbers:

C12.777.829.920/C564042 |C13.351.968.829.920/C564042 |C16.320.322/C564042

Synonyms:

Slim Mappings:

Genetic disease (inborn)|Urogenital disease (female)|Urogenital disease (male)

Reference:

MedGen: C564042
MeSH: C564042
OMIM: 314550;

Genes:

Phenotypes

1	HP:0001417	X-linked inheritance
2	HP:0000076	Vesicoureteral reflux

Disease Causing ClinVar Variants