Adult central nervous system primitive neuroectodermal neoplasm
diseaseOn this page
Also known as adult central nervous system primitive neuroectodermal tumoradult central nervous system primitive neuroectodermal tumouradult central primitive neuroectodermal neoplasmadult central primitive neuroectodermal tumoradult central primitive neuroectodermal tumouradult CNS PNETadult CNS primitive neuroectodermal neoplasmadult CNS primitive neuroectodermal tumoradult CNS primitive neuroectodermal tumourcentral nervous system primitive neuroectodermal neoplasm of adults
Summary
Adult central nervous system primitive neuroectodermal neoplasm (MONDO:0002795) is a cancer. A subtype of central nervous system primitive neuroectodermal 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 | adult central nervous system primitive neuroectodermal neoplasm |
| Mondo ID | MONDO:0002795 |
| DOID | DOID:3865 |
| NCIT | C5411 |
| UMLS | C1332196 |
| MedGen | 231039 |
| GARD | 0027620 |
| Is cancer (heuristic) | yes |
Also known as: adult central nervous system primitive neuroectodermal neoplasm · adult central nervous system primitive neuroectodermal tumor · adult central nervous system primitive neuroectodermal tumour · adult central primitive neuroectodermal neoplasm · adult central primitive neuroectodermal tumor · adult central primitive neuroectodermal tumour · adult CNS PNET · adult CNS primitive neuroectodermal neoplasm · adult CNS primitive neuroectodermal tumor · adult CNS primitive neuroectodermal tumour · central nervous system primitive neuroectodermal neoplasm of adults
Disease family
This is a subtype of central nervous system primitive neuroectodermal 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 › nervous system cancer › central nervous system cancer › central nervous system primitive neuroectodermal neoplasm › adult central nervous system primitive neuroectodermal neoplasm
Related subtypes (7): childhood central nervous system primitive neuroectodermal neoplasm, intracranial primitive neuroectodermal tumor, spinal cord neuroblastoma, ganglioneuroma, spinal cord primitive neuroectodermal tumor, ependymoblastoma, central nervous system tumor with bcor internal tandem duplication
Subtypes (1): adult embryonal tumor with multilayered rosettes, c19mc-altered
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.