ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Familial adenomatous polyposis due to 5q22.2 microdeletion

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:

Familial adenomatous polyposis due to 5q22.2 microdeletion		Epidermolysis bullosa simplex with circinate migratory erythema
	Synonym(s): - Colorectal adenomatous polyposis due to monosomy 5q22.2 - FAP due to monosomy 5q22.2 - Familial adenomatous polyposis due to del(5)(q22.2) - Familial adenomatous polyposis due to monosomy 5q22.2 - Familial polyposis coli due to monosomy 5q22.2		Synonym(s): - EBS-migr

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic 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: No 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
Familial adenomatous polyposis due to 5q22.2 microdeletion
(no data available)