Disease #03498 (CGD-3 (granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3), OMIM:613960)

Global Variome shared LOVD

LOVD v.3.0 Build 25c [ Current LOVD status ]
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Official abbreviation	CGD-3
Name	granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3
OMIM ID	613960
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	NCF4
Associated tissues	-
Disease features	-
Remarks	-