Gonadal disorder
diseaseOn this page
Also known as disease of gonaddisease or disorder of gonaddisorder of gonaddisorder of gonadsgonad diseasegonad disease or disordergonadal disorders
Summary
Gonadal disorder (MONDO:0002259) is a disease (an umbrella term covering 6 Mondo subtypes) and 11 clinical trials. Top therapeutic interventions include testosterone enanthate, avelumab, and finasteride. A subtype of reproductive system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Umbrella term: 6 Mondo subtypes
- Clinical trials: 11
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | gonadal disorder |
| Mondo ID | MONDO:0002259 |
| MeSH | D006058 |
| DOID | DOID:2277 |
| NCIT | C26786 |
| UMLS | C0018050 |
| MedGen | 9074 |
| Anatomy (UBERON) | UBERON:0000991 |
| Is cancer (heuristic) | no |
Also known as: disease of gonad · disease or disorder of gonad · disorder of gonad · disorder of gonads · gonad disease · gonad disease or disorder · gonadal disorder · gonadal disorders
Disease family
This is a subtype of 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 › gonadal disorder
Related subtypes (29): pelvic organ prolapse, cortisone reductase deficiency, physiological sexual disorder, female reproductive system disorder, male reproductive system disorder, pituitary gland disorder, infertility disorder, hypospadias, reproductive system neoplasm, dysplasia of cervix, female genital tuberculosis, habitual spontaneous abortion, aromatase excess syndrome, hand-foot-genital syndrome, mullerian duct anomalies-limb anomalies syndrome, Currarino triad, double uterus-hemivagina-renal agenesis syndrome, congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency, classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency, congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency, spondylocostal dysostosis-anal and genitourinary malformations syndrome, congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency, hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism, estrogen resistance syndrome, short stature, microcephaly, and endocrine dysfunction, diethylstilbestrol syndrome, sexually transmitted disease, NR5A1-related sex development disorder
Subtypes (6): precocious puberty, disorder of sexual differentiation, hypogonadism, testicular disorder, ovarian disorder, gonadoblastoma
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: 11.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE2 | 5 |
| Not specified | 4 |
| PHASE1/PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04460872 | PHASE2 | RECRUITING | Locomotor Training With Testosterone to Promote Bone and Muscle Health After Spinal Cord Injury |
| NCT00947713 | PHASE1/PHASE2 | COMPLETED | Comparison of Micro-dose Human Chorionic Gonadotropin (hCG) With Human Menopausal Gonadotropin (HMG) in Polycystic Ovary Syndrome |
| NCT02248701 | PHASE2 | TERMINATED | Testosterone Plus Finasteride Treatment After Spinal Cord Injury |
| NCT03335254 | PHASE1/PHASE2 | TERMINATED | A Phase 1/2a Study to Determine the Dose Response Pharmacokinetics of TSX-011 (Testosterone Undecanoate) in Hypogonadal Males |
| NCT03403777 | PHASE2 | COMPLETED | Avelumab in Refractory Testicular Germ Cell Cancer. |
| NCT03562897 | PHASE2 | COMPLETED | Evaluation of Ocoxin-Viusid® in Advanced or Metastatic Ovarian Epithelial Cancer |
| NCT04556071 | PHASE2 | UNKNOWN | Efficacy and Safety of Niraparib Combined With Bevacizumab in Platinum Refractory/Resistant Recurrent Ovarian Cancer |
| NCT00202462 | Not specified | COMPLETED | The Effect of Testosterone on Mood and Quality of Life |
| NCT00341458 | Not specified | COMPLETED | Breast Cancer in Poland: An Expanded Study to Assess Occupational and Environmental Factors and Interactions With Genetics |
| NCT00392457 | Not specified | COMPLETED | Investigating the Regulation of Reproductive Hormones in Adult Men |
| NCT05048654 | Not specified | WITHDRAWN | A Novel Ovarian Reserve Monitoring Algorithm for Patients at Risk of Ovarian Injury From Gonadotoxic Therapy |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| TESTOSTERONE ENANTHATE | 4 | 2 |
| AVELUMAB | 4 | 1 |
| FINASTERIDE | 4 | 1 |
| NIRAPARIB | 4 | 1 |
| TESTOSTERONE UNDECANOATE | 4 | 1 |
| CHEMBL4777013 | 0 | 1 |