ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Legius syndrome

Lymphoadenopathic mastocytosis with eosinophilia


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

Citations in the biomedical literature:

Legius syndrome		Lymphoadenopathic mastocytosis with eosinophilia
	Synonym(s): - NF1-like syndrome - Neurofibromatosis 1-like syndrome		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

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

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

No signs/symptoms info available.