ZFIN Human Disease: immunoglobulin alpha deficiency

OBO ID: DOID:0060025

Term Name:	immunoglobulin alpha deficiency		Search Ontology:
Synonyms:	gamma-A-globulin deficiency IgA deficiency
Definition:	A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor. (3)
References:	GARD:10197 MESH:D017098 OMIM:137100 OMIM:269650 OMIM:609529 ORDO:69127 SNOMEDCT_US_2023_03_01:29260007 UMLS_CUI:C0162538
Ontology:	Human Disease ( DOID:0060025 )

Relationships

is a type of:	autosomal recessive disease B cell deficiency autosomal recessive disease B cell deficiency Show first 5 Terms

OTHER immunoglobulin alpha deficiency PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TNFRSF13B		Immunoglobulin A deficiency 2

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None