Jugulotympanic paraganglioma
diseaseOn this page
Also known as basicranium parasympathetic paragangliomaglomus jugulare neoplasmglomus jugulare tumorglomus jugulare tumourGlomus tumorGlomus tumourjugular body neoplasmjugular body neoplasm (disease)jugular body tumorjugular body tumourjugular paragangliomaneoplasm of glomus jugulareneoplasm of jugular bodyneoplasm of the glomus jugulareParaganglioma - glomus jugulareparasympathetic paraganglioma of basicraniumtumor of glomus jugularetumor of jugular bodytumor of the glomus jugulare
Summary
Jugulotympanic paraganglioma (MONDO:0021064) is a disease. A subtype of skull base 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 | jugulotympanic paraganglioma |
| Mondo ID | MONDO:0021064 |
| NCIT | C3061 |
| SNOMED CT | 127030001 |
| UMLS | C0017671 |
| MedGen | 4905 |
| GARD | 0025284 |
| Anatomy (UBERON) | UBERON:0002517 |
| Is cancer (heuristic) | no |
Also known as: basicranium parasympathetic paraganglioma · glomus jugulare neoplasm · glomus jugulare tumor · glomus jugulare tumour · Glomus tumor · Glomus tumour · jugular body neoplasm · jugular body neoplasm (disease) · jugular body tumor · jugular body tumour · jugular paraganglioma · jugulotympanic paraganglioma · neoplasm of glomus jugulare · neoplasm of jugular body · neoplasm of the glomus jugulare · Paraganglioma - glomus jugulare · parasympathetic paraganglioma of basicranium · tumor of glomus jugulare · tumor of jugular body · tumor of the glomus jugulare (+3 more)
Data availability: 2 cell lines.
Disease family
This is a subtype of skull base 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 › head and neck neoplasm › skull neoplasm › skull base neoplasm › jugulotympanic paraganglioma
Related subtypes (4): sella turcica neoplasm, skull base chordoma, skull base meningioma, sphenoidal sinus neoplasm
Subtypes (1): malignant jugulotympanic paraganglioma
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.