Human Phenotype Ontology

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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

..Starting node
..High-grade vesicoureteral reflux (HP:0033734)

Term ID:

33734

Name:

High-grade vesicoureteral reflux

Synonym:

Definition:

Vesicoureteral reflux with dilation of the renal calyces (Grade III - V).

Comments:

Reference:

HP:0033734

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0033734	HP:0033734	High-grade vesicoureteral reflux	0	ZMYM2 CL E G H	7750	12989	OMIM:619522	NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC
HP:0033734	HP:0033740	Grade V vesicoureteral reflux	1	CL E G H
HP:0033734	HP:0033742	Intrarenal reflux	1	CL E G H
HP:0033734	HP:0033741	Grade IV vesicoureteral reflux	1	CL E G H
HP:0033734	HP:0033737	Grade III vesicoureteral reflux	1	ZMYM2 CL E G H	7750	12989	OMIM:619522	NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC

Genes (1) :ZMYM2

Diseases (1) :OMIM:619522

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.