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Keratosis palmoplantaris striata

3 OMIM references -
3 associated genes
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Primary systemic amyloidosis

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

Keratosis palmoplantaris striata

Primary systemic amyloidosis

DSG1	(UniProt - OMIM)		APOA1	(UniProt - OMIM)
DSP	(UniProt - OMIM)
KRT1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KRT1	(0.72)	APOA1

Citations in the biomedical literature:

Keratosis palmoplantaris striata		Primary systemic amyloidosis
	Synonym(s): - Keratosis palmoplantaris striata et areata - Keratosis palmoplantaris varians of Wachters - Striate palmoplantar keratoderma		Synonym(s): - Systemic AL amyloidosis - Systemic immunoglobulinic amyloidosis

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare hematologic disease - Rare neurologic disease - Rare oncologic disease - Rare renal disease - Rare systemic or rheumatologic disease

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

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