ODCs

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3 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
6 signs/symptoms

Autoimmune lymphoproliferative syndrome

Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CASP10	(0.52)	DSP

Citations in the biomedical literature:

Autoimmune lymphoproliferative syndrome		Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
	Synonym(s): - ALPS - Canale-Smith syndrome - FAS deficiency		Synonym(s): - Carvajal syndrome - Woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome - Wooly hair - palmoplantar keratoderma - dilated cardiomyopathy - Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare immune disease - Rare oncologic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 3 OMIM references - 1 MeSH reference: D056735		External references: 1 OMIM reference - No MeSH references

Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
	Very frequent - Autosomal recessive inheritance - Cardiomyopathy / hypertrophic / dilated - Palmoplantar hyperkeratosis / keratoderma - Woolly / frizzy hair Occasional - Heart / cardiac failure - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment
Autoimmune lymphoproliferative syndrome
(no data available)