ODCs

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1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 2

4 OMIM references -
4 associated genes
No signs/symptoms info

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIT KIT	(0.73) (0.52)	PTPRO PLCE1

Citations in the biomedical literature:

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease		Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the genitourinary system -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 4 OMIM references - No MeSH references

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
	Very frequent - Acute leukemia - Eosinophils anomalies / hypereosinophilia - Mastocytosis - Myeloproliferative syndrome / chronic leukemia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
(no data available)