Fixed pigmented erythema

disease
On this page

Also known as fixed drug eruption

Summary

Fixed pigmented erythema (MONDO:0017395) is a disease. A subtype of toxic dermatosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: Unknown (Worldwide) [Orphanet-validated]
  • Phenotypes (HPO): 18

Clinical features

Signs & symptoms

Clinical features (HPO)

18 HPO clinical features (Orphanet curated; top 18 by frequency):

HPO IDTermFrequency
HP:0010783ErythemaVery frequent (80-99%)
HP:0020172Adverse drug responseVery frequent (80-99%)
HP:0410323Drug allergyVery frequent (80-99%)
HP:0011356Regional abnormality of skinFrequent (30-79%)
HP:0025474Erythematous plaqueFrequent (30-79%)
HP:0003341Junctional splitFrequent (30-79%)
HP:0000953Hyperpigmentation of the skinOccasional (5-29%)
HP:0000155Oral ulcerOccasional (5-29%)
HP:0010280StomatitisOccasional (5-29%)
HP:0008066Abnormal blistering of the skinOccasional (5-29%)
HP:0200041Skin erosionOccasional (5-29%)
HP:0032156Skin detachmentOccasional (5-29%)
HP:0001945FeverOccasional (5-29%)
HP:0012378FatigueOccasional (5-29%)
HP:0011354Generalized abnormality of skinVery rare (<1-4%)
HP:0007473Crusting erythematous dermatitisVery rare (<1-4%)
HP:0032565Vaginal mucosal ulcerationVery rare (<1-4%)
HP:0025143ChillsVery rare (<1-4%)

Identifiers

Disease identifiers

FieldValue
Canonical namefixed pigmented erythema
Mondo IDMONDO:0017395
Orphanet293812
ICD-1120014644
SNOMED CT73692007
UMLSC0221242
MedGen526203
GARD0021170
MedDRA10048796
Is cancer (heuristic)no

Also known as: fixed drug eruption

Disease family

Classification path: disease › human disease › disease by body system or component › integumentary system disorder › skin disorder › toxic dermatosis › fixed pigmented erythema

Related subtypes (4): drug rash with eosinophilia and systemic symptoms, acute generalized exanthematous pustulosis, toxic epidermal necrolysis, erythema multiforme major

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.