ODCs

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1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

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

Legius syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KIT	(0.59)	SPRED1

Citations in the biomedical literature:

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease		Legius syndrome
	Synonym(s): (no synonyms)		Synonym(s): - NF1-like syndrome - Neurofibromatosis 1-like syndrome

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

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

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C548032

Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
	Very frequent - Acute leukemia - Eosinophils anomalies / hypereosinophilia - Mastocytosis - Myeloproliferative syndrome / chronic leukemia
Legius syndrome
(no data available)