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autosomal recessive chronic granulomatous disease cytochrome b-positive type I (DOID:0070192)
Alliance: disease page
Synonyms: CDG1; chronic granulomatous disease due to deficiency of NCF-1; deficiency of NCF1; deficiency of neutrophil cytosol factor 1; deficiency of p47-PHOX; deficiency of SOC2; deficiency of soluble oxidase component II
Alt IDs: OMIM:233700
Definition: A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF1 gene on chromosome 7q11.23.


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
02/11/2020
MGI 6.14
The Jackson Laboratory