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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
Familial capillary hemangioma
1 OMIM reference -
2 associated genes
No signs/symptoms info
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Familial capillary hemangioma

PLCG2
(UniProt - OMIM)
 ANTXR1
(UniProt - OMIM)
KDR
(UniProt - OMIM)

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


Citations in the biomedical literature:


Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
PLCG2
Familial capillary hemangioma
ANTXR1 KDR



Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Familial capillary hemangioma

Synonym(s):
- aPLAID
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic 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:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.