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Keratosis palmoplantaris striata

3 OMIM references -
3 associated genes
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Congenital analbuminemia

1 associated gene
No signs/symptoms info

Keratosis palmoplantaris striata

Congenital analbuminemia

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


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

Citations in the biomedical literature:

Keratosis palmoplantaris striata		Congenital analbuminemia
	Synonym(s): - Keratosis palmoplantaris striata et areata - Keratosis palmoplantaris varians of Wachters - Striate palmoplantar keratoderma		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: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		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: 3 OMIM references - No MeSH references		External references: No 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)