ODCs

Cytoscape Web

Click node...

Idiopathic hypereosinophilic syndrome

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

PROTEIN INTERACTIONS: 1

Bullous diffuse cutaneous mastocytosis

1 associated gene
7 signs/symptoms

Idiopathic hypereosinophilic syndrome

Bullous diffuse cutaneous mastocytosis

FIP1L1	(UniProt - OMIM)		KIT	(UniProt - OMIM)
PDGFRA	(UniProt - OMIM)
PDGFRB	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PDGFRA	(0.63)	KIT

Citations in the biomedical literature:

Idiopathic hypereosinophilic syndrome		Bullous diffuse cutaneous mastocytosis
	Synonym(s): (no synonyms)		Synonym(s): - Bullous DCM

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic

	External references: 1 OMIM reference - 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
Idiopathic hypereosinophilic syndrome
(no data available)