ODCs

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

COMMON GENES: 1

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

Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation

PLCG2-associated antibody deficiency and immune dysregulation

Citations in the biomedical literature:

Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation		PLCG2-associated antibody deficiency and immune dysregulation
	Synonym(s): - aPLAID		Synonym(s): - FACU - Familial atypical cold urticaria - Familial cold urticaria with common variable immunodeficiency - PLAID

	Classification (Orphanet): - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare allergic disease - Rare genetic disease - Rare immune disease - Rare skin disease - Rare systemic or rheumatologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	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: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.