stromal predominant kidney Wilms tumor
diseaseOn this page
Also known as stromal predominant kidney adenosarcomastromal predominant kidney Wilms' tumorstromal predominant nephroblastomastromal predominant renal adenosarcomastromal predominant renal Wilm's tumorstromal predominant renal Wilm's tumourstromal predominant renal Wilms tumorstromal predominant renal Wilms' tumorstromal predominant renal Wilms' tumourstromal predominant Wilms tumorstromal predominant Wilms tumour
Summary
stromal predominant kidney Wilms tumor (MONDO:0006432) is a cancer. A subtype of kidney Wilms tumor — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | stromal predominant kidney Wilms tumor |
| Mondo ID | MONDO:0006432 |
| DOID | DOID:5191 |
| NCIT | C9148 |
| UMLS | C0279610 |
| MedGen | 83529 |
| GARD | 0024411 |
| Is cancer (heuristic) | yes |
Also known as: stromal predominant kidney adenosarcoma · stromal predominant kidney Wilms tumor · stromal predominant kidney Wilms’ tumor · stromal predominant nephroblastoma · stromal predominant renal adenosarcoma · stromal predominant renal Wilm’s tumor · stromal predominant renal Wilm’s tumour · stromal predominant renal Wilms tumor · stromal predominant renal Wilms’ tumor · stromal predominant renal Wilms’ tumour · stromal predominant Wilms tumor · stromal predominant Wilms tumour
Disease family
This is a subtype of kidney Wilms tumor. 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 › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › malignant urinary system neoplasm › kidney cancer › kidney Wilms tumor › stromal predominant kidney Wilms tumor
Related subtypes (7): nonanaplastic kidney Wilms tumor, metachronous kidney Wilms’ tumor, mixed cell type kidney Wilms’ tumor, blastema predominant kidney Wilms tumor, epithelial predominant Wilms’ tumor, adult kidney Wilms tumor, childhood kidney Wilms tumor
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.