ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Annular epidermolytic ichthyosis

Hereditary angioedema type 3

KRT1	(UniProt - OMIM)		F12	(UniProt - OMIM)
KRT10	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT1	(0.52)	F12

Citations in the biomedical literature:

Annular epidermolytic ichthyosis		Hereditary angioedema type 3
	Synonym(s): - AEI		Synonym(s): - HAE 3 - HAE-III - Hereditary angioneurotic edema type 3 - Inherited estrogen-associated angioedema - Inherited estrogen-associated angioneurotic edema - Inherited estrogen-dependent angioedema - Inherited estrogen-dependent angioneurotic edema

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare allergic disease - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D056828

No signs/symptoms info available.