Primitive neuroectodermal tumor of the cervix uteri
disease diseaseOn this page
Also known as cervical malignant peripheral neuroectodermal tumorcervical malignant peripheral neuroectodermal tumourcervical peripheral neuroectodermal cancermalignant peripheral neuroectodermal tumor of the cervix uterimalignant peripheral neuroectodermal tumour of the cervix uteriperipheral neuroectodermal cancer of cervix uteri
Summary
Primitive neuroectodermal tumor of the cervix uteri (MONDO:0016284) is a cancer. A subtype of sarcoma of cervix uteri — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Classification: Cancer
- Prevalence: <1 / 1 000 000 (Worldwide) [Orphanet-validated]
Clinical features
Epidemiology
Prevalence records
1 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | Worldwide | Validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | primitive neuroectodermal tumor of the cervix uteri |
| Mondo ID | MONDO:0016284 |
| Orphanet | 213812 |
| UMLS | C4707725 |
| MedGen | 1636418 |
| GARD | 0020496 |
| Is cancer (heuristic) | yes |
Also known as: cervical malignant peripheral neuroectodermal tumor · cervical malignant peripheral neuroectodermal tumour · cervical peripheral neuroectodermal cancer · malignant peripheral neuroectodermal tumor of the cervix uteri · malignant peripheral neuroectodermal tumour of the cervix uteri · peripheral neuroectodermal cancer of cervix uteri
Disease family
This is a subtype of sarcoma of cervix uteri. 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 by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › cancer › reproductive system cancer › female reproductive organ cancer › uterine cancer › cervical cancer › sarcoma of cervix uteri › primitive neuroectodermal tumor of the cervix uteri
Related subtypes (4): cervical alveolar soft part sarcoma, endometrioid stromal sarcoma of the cervix, rhabdomyosarcoma of the cervix uteri, leiomyosarcoma of the cervix uteri
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.