ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Gardner syndrome

Epidermolysis bullosa simplex with circinate migratory erythema


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APC	(0.63)	KRT5

Citations in the biomedical literature:

Gardner syndrome		Epidermolysis bullosa simplex with circinate migratory erythema
	Synonym(s): (no synonyms)		Synonym(s): - EBS-migr

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D005736		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
Gardner syndrome
(no data available)