Male reproductive system neoplasm

Summary

Male reproductive system neoplasm (MONDO:0024582) is a cancer (an umbrella term covering 6 Mondo subtypes). A subtype of male reproductive system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer
• Umbrella term: 6 Mondo subtypes

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	male reproductive system neoplasm
Mondo ID	MONDO:0024582
NCIT	C3054
SNOMED CT	126895004
UMLS	C0017417
MedGen	42196
Anatomy (UBERON)	UBERON:0003135
Is cancer (heuristic)	yes

Also known as: male reproductive organ neoplasm · male reproductive organ tumor · male reproductive organ tumour · Male reproductive system neoplasm · Male reproductive system tumor · Male reproductive system tumour · neoplasm of male reproductive organ · neoplasm of Male reproductive system · neoplasm of the Male reproductive system · tumor of male reproductive organ · tumor of Male reproductive system · tumor of the Male reproductive system · tumour of male reproductive organ · tumour of Male reproductive system · tumour of the Male reproductive system

Disease family

This is a subtype of male reproductive system disorder. 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 › reproductive system disorder › male reproductive system disorder › male reproductive system neoplasm

Related subtypes (25): benign male reproductive system neoplasm, hematocele of tunica vaginalis testis, male genital organ stricture, male genital organ vascular disease, penile disorder, testicular disorder, prostate disorder, epididymitis, hydrocele, male infertility, male genital tuberculosis, spermatocele, dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome, cryptorchidism, diphallia, postorgasmic illness syndrome, penoscrotal transposition, congenital bilateral absence of vas deferens, posterior hypospadias, isolated micropenis, fournier gangrene, congenital agenesis of the scrotum, scrotal disorder, congenital megaprepuce, epididymis disease

Subtypes (6): lipoma of spermatic cord, epididymal neoplasm, scrotum neoplasm, male reproductive organ cancer, penile neoplasm, neoplasm of testis

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.