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Bullous diffuse cutaneous mastocytosis

1 associated gene
7 signs/symptoms

PROTEIN INTERACTIONS: 1

Familial progressive hyperpigmentation

3 OMIM references -
1 associated gene
No signs/symptoms info

Bullous diffuse cutaneous mastocytosis

Familial progressive hyperpigmentation

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIT	(0.9)	KITLG

Citations in the biomedical literature:

Bullous diffuse cutaneous mastocytosis		Familial progressive hyperpigmentation
	Synonym(s): - Bullous DCM		Synonym(s): - Melanosis diffusa congenita - Melanosis universalis hereditaria - Universal melanosis

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy 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: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

Bullous diffuse cutaneous mastocytosis
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Mastocytosis - Pruritus / itching - Urticaria - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Occasional - Collapse / sudden death / cardiac arrest / cardiorespiratory arrest
Familial progressive hyperpigmentation
(no data available)