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Disease Ontology Browser
immunodeficiency 80 (DOID:0061051)
Alliance: disease page
Synonyms: immunodeficiency 80 with or without cautosomal recessive inheritancediomyopathy
Alt IDs: OMIM:619313
Definition: A primary immunodeficiency disease that is characterized by variable manifestations and that has_material_basis_in compound heterozygous mutation in the MCM10 gene on chromosome 10p13.

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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory