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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Disseminated superficial actinic porokeratosis

5 OMIM references -
1 associated gene
8 signs/symptoms

Ewing sarcoma

Disseminated superficial actinic porokeratosis

ERG	(UniProt - OMIM)		MVK	(UniProt - OMIM)
ETV1	(UniProt - OMIM)
ETV4	(UniProt - OMIM)
EWSR1	(UniProt - OMIM)
FLI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EWSR1	(0.73)	MVK

Citations in the biomedical literature:

Ewing sarcoma		Disseminated superficial actinic porokeratosis

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - No MeSH references

Disseminated superficial actinic porokeratosis
	Very frequent - Follicular / erythematous / edematous papules / milium - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Hypohidrosis / decreased sweating / thermoregulation disorder / heat intolerance - Skin hypoplasia / aplasia / atrophy Frequent - Pruritus / itching - Skin photosensitivity Occasional - Autosomal dominant inheritance - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma)
Ewing sarcoma
(no data available)