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Epidermolytic palmoplantar keratoderma

1 OMIM reference -
4 associated genes
8 signs/symptoms

PROTEIN INTERACTIONS: 3

Congenital analbuminemia

1 associated gene
No signs/symptoms info

Epidermolytic palmoplantar keratoderma

Congenital analbuminemia

KRT1	(UniProt - OMIM)		ALB	(UniProt - OMIM)
KRT16	(UniProt - OMIM)
KRT6C	(UniProt - OMIM)
KRT9	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT1 KRT16 KRT9	(0.72) (0.72) (0.72)	ALB ALB ALB

Citations in the biomedical literature:

Epidermolytic palmoplantar keratoderma		Congenital analbuminemia
	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): (no synonyms)

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

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

Epidermolytic palmoplantar keratoderma
	Very frequent - Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Palmoplantar hyperkeratosis / keratoderma - Warts / papillomas Frequent - Abnormal fingernails - Eczema - Hyperhidrosis / increased sweating
Congenital analbuminemia
(no data available)