ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Progressive symmetric erythrokeratodermia

Exfoliative ichthyosis


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

Citations in the biomedical literature:

Progressive symmetric erythrokeratodermia		Exfoliative ichthyosis
	Synonym(s): - Darier-Gottron disease - Progressiva symmetrica erythrokeratodermia - Progressive symmetric erythrokeratodermia, Gottron type		Synonym(s): - Autosomal recessive exfoliative ichthyosis - Ichthyosis exfoliativa

	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: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

Progressive symmetric erythrokeratodermia
	Very frequent - Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Palmoplantar hyperkeratosis / keratoderma
Exfoliative ichthyosis
(no data available)