Malignant prostate phyllodes tumor

Summary

Malignant prostate phyllodes tumor (MONDO:0000994) is a cancer. A subtype of malignant urinary system neoplasm — 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	malignant prostate phyllodes tumor
Mondo ID	MONDO:0000994
DOID	DOID:10289
NCIT	C5531
UMLS	C1334615
MedGen	235301
GARD	0022859
Is cancer (heuristic)	yes

Also known as: malignant phyllodes neoplasm of prostate · malignant phyllodes neoplasm of the prostate · malignant phyllodes tumor of prostate · malignant phyllodes tumor of the prostate · malignant phyllodes tumour of prostate · malignant phyllodes tumour of the prostate · malignant prostate phyllodes neoplasm · malignant prostate phyllodes tumor · prostate malignant phyllodes tumour

Disease family

This is a subtype of malignant urinary system neoplasm. 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 › malignant prostate phyllodes tumor

Related subtypes (9): urinary bladder cancer, kidney cancer, urethra cancer, multiple endocrine neoplasia type 2B, ureter cancer, pheochromocytoma/paraganglioma syndrome 2, pheochromocytoma/paraganglioma syndrome 5, infiltrating urothelial carcinoma, urothelial carcinoma

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.