granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
Go to external page http://purl.obolibrary.org/obo/MONDO_0009310
Any chronic granulomatous disease in which the cause of the disease is a mutation in the NCF2 gene. [ MONDO:patterns/disease_series_by_gene ]
Term information
- UMLS:C1856245 (OMIM:233710)
- DOID:0070191 (MONDO:equivalentTo)
- OMIM:233710 (MONDO:equivalentTo)
- MESH:C565531 (MONDO:equivalentTo)
http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml
Any chronic granulomatous disease in which the cause of the disease is a mutation in the NCF2 gene.
http://purl.obolibrary.org/obo/DOID_0070191
http://identifiers.org/omim/233710
http://identifiers.org/mesh/C565531
http://linkedlifedata.com/resource/umls/id/C1856245
chronic granulomatous disease caused by mutation in NCF2
NCF2 chronic granulomatous disease
granulomatous disease, chronic, due to Ncf2 deficiency
neutrophil cytosol Factor 2, deficiency of
CDG2
granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type II
Ncf2, deficiency of
CGD, autosomal recessive cytochrome B-positive, type 2
P67-PHOX, deficiency of