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Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

SSR4-CDG

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POMP	(0.63)	SSR4

Citations in the biomedical literature:

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome		SSR4-CDG
	Synonym(s): - KLICK syndrome		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Inborn errors of metabolism - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

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

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
	Very frequent - Autosomal dominant inheritance - Ichthyosis / ichthyosiform dermatitis - Palmoplantar hyperkeratosis / keratoderma Frequent - Joint / articular deformation
SSR4-CDG
(no data available)