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Disease Ontology Browser
autosomal recessive chronic granulomatous disease cytochrome b-positive type II (DOID:0070191)
Alliance: disease page
Synonyms: CDG2; chronic granulomatous disease due to deficiency of NCF-2; deficiency of NCF2; deficiency of p67-PHOX
Alt IDs: OMIM:233710
Definition: A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25.


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
02/18/2020
MGI 6.14
The Jackson Laboratory