ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Exfoliative ichthyosis

Keratoderma hereditarium mutilans with ichthyosis


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

Citations in the biomedical literature:

Exfoliative ichthyosis		Keratoderma hereditarium mutilans with ichthyosis
	Synonym(s): - Autosomal recessive exfoliative ichthyosis - Ichthyosis exfoliativa		Synonym(s): - Camisa disease - Keratoderma - ichthyosiform dermatosis - elevated beta-glucuronidase - Loricrin keratoderma - Vohwinkel syndrome - ichthyosis

	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: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

Keratoderma hereditarium mutilans with ichthyosis
	Very frequent - Ichthyosis / ichthyosiform dermatitis - Palmoplantar hyperkeratosis / keratoderma Occasional - Auto-aggressivity / auto-mutilation - Hypertonia / spasticity / rigidity / stiffness - Motor deficit / trouble - Nails anomalies
Exfoliative ichthyosis
(no data available)