Benign hypertensive renal disease
disease diseaseOn this page
Also known as hypertensive renal disease, benignhypertensive renal disease, benign, without mention of renal failure
Summary
Benign hypertensive renal disease (MONDO:0001304) is a disease. A subtype of hypertensive nephropathy — 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 | benign hypertensive renal disease |
| Mondo ID | MONDO:0001304 |
| DOID | DOID:11520 |
| SNOMED CT | 193003 |
| UMLS | C0155596 |
| MedGen | 510035 |
| Is cancer (heuristic) | no |
Also known as: hypertensive renal disease, benign · hypertensive renal disease, benign, without mention of renal failure
Disease family
This is a subtype of hypertensive nephropathy. 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 body system or component › urinary system disorder › kidney disorder › hypertensive nephropathy › benign hypertensive renal disease
Related subtypes (1): malignant hypertensive renal disease
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.