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Disease Ontology Browser
autosomal recessive dyskeratosis congenita 2 (DOID:0070017)
Alliance: disease page
Synonyms: DKCB2
Alt IDs: OMIM:613987
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of NOLA2 on chromosome 5q35.3.


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
10/08/2019
MGI 6.14
The Jackson Laboratory