ODCs

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1 OMIM reference -
4 associated genes
8 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3

1 OMIM reference -
1 associated gene
3 signs/symptoms

Epidermolytic palmoplantar keratoderma

Progressive symmetric erythrokeratodermia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT1	(0.75)	LOR

Citations in the biomedical literature:

Epidermolytic palmoplantar keratoderma		Progressive symmetric erythrokeratodermia
	Synonym(s): - Diffuse erythrodermic palmoplantar keratoderma, Voerner type - Diffuse erythrodermic palmoplantar keratoderma, VÃ¶rner type - EPPK - Epidermolytic palmoplantar keratoderma of Voerner - Epidermolytic palmoplantar keratoderma of VÃ¶rner		Synonym(s): - Darier-Gottron disease - Progressiva symmetrica erythrokeratodermia - Progressive symmetric erythrokeratodermia, Gottron type

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		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: normal Type of inheritance: autosomal dominant

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


COMMON SIGNS	- Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Palmoplantar hyperkeratosis / keratoderma

Epidermolytic palmoplantar keratoderma		Progressive symmetric erythrokeratodermia
	Very frequent - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Warts / papillomas Frequent - Abnormal fingernails - Eczema - Hyperhidrosis / increased sweating		(no more signs)