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| Term | immunodeficiency 89 | ID (Ontology) | DOID:0061059 (Human Disease) |
| Definition | A primary immunodeficiency disease that is characterized by adult onset of recurrent infections, allergies, microcytic anemia, and Crohn disease and that has_material_basis_in homozygous mutation in the CARD10 gene on chromosome 22q13. | ||
| Also Known As | "immunodeficiency 89 and autoimmunity" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal recessive disease_______ immune system disease | |__primary immunodeficiency disease__| immunodeficiency 89 |
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autosomal recessive disease primary immunodeficiency disease |
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| MIM:619632 | |||