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
..Grade II vesicoureteral reflux (HP:0033736)

Term ID:

33736

Name:

Grade II vesicoureteral reflux

Synonym:

Grade II VUR; VUR II

Definition:

Vesicoureteral reflux into a non-dilated pyelocalyceal system.

Comments:

Reference:

HP:0033736

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:0033736	HP:0033736	Grade II vesicoureteral reflux	0	UNC45A CL E G H	55898	30594	OMIM:619377	OSTEOOTOHEPATOENTERIC SYNDROME; OOHE

Genes (1) :UNC45A

Diseases (1) :OMIM:619377

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