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immunodeficiency 99 (DOID:0061069)
Alliance: disease page
Synonyms: immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias
Alt IDs: OMIM:619846
Definition: A combined T cell and B cell immunodeficiency that is characterized by the onset of recurrent sinopulmonary infections in early childhood and that has_material_basis_in homozygous mutation in the CTNNBL1 gene on chromosome 20q11.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory