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Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive lymphoproliferative disease
2 OMIM references -
2 associated genes
No signs/symptoms info
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Autosomal recessive lymphoproliferative disease

PLCG2
(UniProt - OMIM)
 CD27
(UniProt - OMIM)
ITK
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PLCG2
(0.52)
ITK


Citations in the biomedical literature:


Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
PLCG2
Autosomal recessive lymphoproliferative disease
CD27 ITK



Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Autosomal recessive lymphoproliferative disease

Synonym(s):
- aPLAID
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.