About   Help   FAQ
Disease Ontology Browser
autosomal recessive chronic granulomatous disease 1 (DOID:0070192)
Alliance: disease page
Synonyms: autosomal recessive chronic granulomatous disease cytochrome b-positive type I; 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory