Disease #00654

Official abbreviation	613960
Name	Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III
OMIM ID	613960
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	NCF4
Associated tissues	-
Disease features	-
Remarks	-