ODCs

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4 OMIM references -
3 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Dowling-Degos disease

Epidermolysis bullosa simplex with circinate migratory erythema

Citations in the biomedical literature:

Dowling-Degos disease		Epidermolysis bullosa simplex with circinate migratory erythema
	Synonym(s): - Reticular pigment anomaly of flexures		Synonym(s): - EBS-migr

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Epidermolysis bullosa simplex with circinate migratory erythema
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Cutaneous rash - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment
Dowling-Degos disease
(no data available)