NCF4

Name: NCF4
HGNC ID: HGNC:7662
Cytogenetic Location: 22q12.3
Haploinsufficiency: Associated with Autosomal Recessive Phenotype

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ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

NCF4 - granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3 | MONDO:0013507

Curated by	Classification		Date	Report
Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype		06/01/2017	View report

NCF4

Curated by	Classification		Date	Report
Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype		06/01/2017	View report