Vesicoureteral reflux 1

Summary

Vesicoureteral reflux 1 (MONDO:0008653) is a disease. A subtype of familial vesicoureteral reflux — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	vesicoureteral reflux 1
Mondo ID	MONDO:0008653
OMIM	193000
UMLS	C4551858
MedGen	1644868
GARD	0018418
Is cancer (heuristic)	no

Also known as: vesicoureteral reflux 1 · VUR1

Disease family

This is a subtype of familial vesicoureteral reflux. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › disease of genetic or genomic mechanism › hereditary disease › familial vesicoureteral reflux › vesicoureteral reflux 1

Related subtypes (8): vesicoureteral reflux, X-linked, vesicoureteral reflux 2, vesicoureteral reflux 3, vesicoureteral reflux 4, vesicoureteral reflux 5, vesicoureteral reflux 6, vesicoureteral reflux 7, vesicoureteral reflux 8

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 0.