ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
4 signs/symptoms

Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation

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


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PLCG2	(0.72)	KIT

Citations in the biomedical literature:

Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation		Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
	Synonym(s): - aPLAID		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	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: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: sporadic

	External references: 1 OMIM reference - No MeSH references		External references: No 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
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
(no data available)