Disease #01831 (CGD1 (granulomatous disease, chronic, due to deficiency of NCF-1, type 1), OMIM:233700)

Official abbreviation CGD1
Name granulomatous disease, chronic, due to deficiency of NCF-1, type 1
OMIM ID 233700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NCF1
Associated tissues -
Disease features -
Remarks -