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| Term | immunoglobulin alpha deficiency | ID (Ontology) | DOID:0060025 (Human Disease) |
| Definition | A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor. | ||
| Also Known As | "gamma-A-globulin deficiency" ; "IgA deficiency" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease___ primary immunodeficiency disease | |__B cell deficiency_____________| immunoglobulin alpha deficiency |
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Relationships
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| Is a |
autosomal recessive disease B cell deficiency |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:10197 MESH:D017098 MIM:137100 MIM:269650 MIM:609529 ORDO:69127 SNOMEDCT_US_2023_03_01:29260007 UMLS_CUI:C0162538 |
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