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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

PLCG2 KIT


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
PLCG2
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
KIT



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)