Cervix squamous papilloma

Summary

Cervix squamous papilloma (MONDO:0004788) is a disease. A subtype of cervical benign 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	cervix squamous papilloma
Mondo ID	MONDO:0004788
DOID	DOID:9445
NCIT	C6342
UMLS	C1336900
MedGen	237038
Anatomy (UBERON)	UBERON:0000002
Is cancer (heuristic)	no

Also known as: cervical squamous papilloma · cervix squamous papilloma · cervix uteri squamous papilloma · squamous papilloma of cervix · squamous papilloma of cervix uteri · squamous papilloma of the cervix · squamous papilloma of the cervix uteri · squamous papilloma of the uterine cervix · squamous papilloma of uterine cervix · uterine cervix squamous papilloma

Disease family

This is a subtype of cervical benign 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: human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › benign neoplasm › benign reproductive system neoplasm › benign female reproductive system neoplasm › uterine benign neoplasm › cervical benign neoplasm › cervix squamous papilloma

Related subtypes (3): cervical adenofibroma, cervical mullerian papilloma, benign uterine ligament neoplasm

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.