ODCs

Cytoscape Web

Click node...

Familial progressive hyper- and hypopigmentation

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Bullous diffuse cutaneous mastocytosis

1 associated gene
7 signs/symptoms

Familial progressive hyper- and hypopigmentation

Bullous diffuse cutaneous mastocytosis

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Familial progressive hyper- and hypopigmentation		Bullous diffuse cutaneous mastocytosis
	Synonym(s): - FPHH		Synonym(s): - Bullous DCM

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy 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: - Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: No 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 hyper- and hypopigmentation
(no data available)