Cutaneous syphilis

Summary

Cutaneous syphilis (MONDO:0006718) is a disease. A subtype of syphilis — 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	cutaneous syphilis
Mondo ID	MONDO:0006718
EFO	EFO:1000887
MeSH	D013591
UMLS	C0039132
MedGen	52623
GARD	0027763
Anatomy (UBERON)	UBERON:0000014
Is cancer (heuristic)	no

Also known as: Treponema pallidum caused skin disease caused by bacterial infection · Treponema pallidum skin disease caused by bacterial infection

Disease family

This is a subtype of syphilis. 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 › disease of primarily extrinsic mechanism › infectious disease › bacterial infectious disease › primary bacterial infectious disease › syphilis › cutaneous syphilis

Related subtypes (9): bejel, primary syphilis, secondary syphilis, tertiary syphilis, congenital syphilis, latent syphilis, yaws, syphilitic aortitis, chancre

Subtypes (1): late yaws

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.