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Congenital analbuminemia

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Keratosis palmoplantaris striata

3 OMIM references -
3 associated genes
4 signs/symptoms

Congenital analbuminemia

Keratosis palmoplantaris striata

ALB	(UniProt - OMIM)		DSG1	(UniProt - OMIM)
			DSP	(UniProt - OMIM)
			KRT1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Congenital analbuminemia		Keratosis palmoplantaris striata
	Synonym(s): (no synonyms)		Synonym(s): - Keratosis palmoplantaris striata et areata - Keratosis palmoplantaris varians of Wachters - Striate palmoplantar keratoderma

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

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

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

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

Keratosis palmoplantaris striata
	Very frequent - Autosomal dominant inheritance - Palmoplantar hyperkeratosis / keratoderma Frequent - Hair and scalp anomalies - Nails anomalies
Congenital analbuminemia
(no data available)