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| Term | immunodeficiency 125 | ID (Ontology) | DOID:0061091 (Human Disease) |
| Definition | A B cell deficiency that is characterized by recurrent diarrhea and failure to thrive beginning in infancy followed by recurrent bacterial, viral, and fungal infections and that has_material_basis_in homozygous mutation in the FLT3LG gene on chromosome 19q13. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease___ primary immunodeficiency disease | |__B cell deficiency_____________| immunodeficiency 125 |
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| Is a |
autosomal recessive disease B cell deficiency |
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External Crossreferences & Linkouts
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| MIM:620926 | |||