Testicular gonadoblastoma
diseaseOn this page
Also known as gonadoblastoma of testistesticular gonadoblastoma (disease)testis gonadoblastoma
Summary
Testicular gonadoblastoma (MONDO:0002698) is a disease. A subtype of testicular sex cord-stromal neoplasm — 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 | testicular gonadoblastoma |
| Mondo ID | MONDO:0002698 |
| DOID | DOID:3579 |
| NCIT | C39911 |
| UMLS | C1515283 |
| MedGen | 272839 |
| GARD | 0023215 |
| Anatomy (UBERON) | UBERON:0000473 |
| Is cancer (heuristic) | no |
Also known as: gonadoblastoma of testis · testicular gonadoblastoma · testicular gonadoblastoma (disease) · testis gonadoblastoma
Data availability: 1 HPO phenotype.
Disease family
Classification path: disease › human disease › disease by body system or component › reproductive system disorder › reproductive system neoplasm › sex cord-stromal tumor › testicular sex cord-stromal neoplasm › testicular gonadoblastoma
Related subtypes (9): testicular lymphoma, Sertoli-Leydig cell tumor, testicular Leydig cell tumor, testicular granulosa cell tumor, testicular fibroma, testicular thecoma, testicular sertoli cell tumor, testicular fibrothecoma, testicular sex cord-stromal benign neoplasm
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.