Calcified aponeurotic fibroma
disease diseaseOn this page
Also known as Juvenile aponeurotic fibromajuvenile aponeurotic fibromatosisJuvenile aponeurotic fibrosisKeasby tumorKeasby tumour
Summary
Calcified aponeurotic fibroma (MONDO:0016038) is a disease. A subtype of fibroma — 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 | calcified aponeurotic fibroma |
| Mondo ID | MONDO:0016038 |
| Orphanet | 199260 |
| NCIT | C4818 |
| SNOMED CT | 703614006 |
| UMLS | C0553647 |
| MedGen | 107818 |
| GARD | 0020329 |
| Is cancer (heuristic) | no |
Also known as: Juvenile aponeurotic fibroma · juvenile aponeurotic fibromatosis · Juvenile aponeurotic fibrosis · Keasby tumor · Keasby tumour
Disease family
Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › mesenchymal cell neoplasm › fibroblastic neoplasm › fibroma › calcified aponeurotic fibroma
Related subtypes (10): testicular fibroma, liver solitary fibrous tumor, serous cystadenofibroma, adenofibroma, tendon sheath fibroma, uterine corpus leiomyoma, ovarian fibroma, fibroma of lung, fibroma of prostate, oral fibroma
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.