MOCS2

Name: MOCS2
HGNC ID: HGNC:7193
Cytogenetic Location: 5q11.2
Haploinsufficiency: Associated with Autosomal Recessive Phenotype
Triplosensitivity: No Evidence

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MOCS2 - sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | MONDO:0009644

Curated by	Classification		Date	Report
Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype		10/25/2018	View report

MOCS2

Curated by	Classification		Date	Report
Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype		10/25/2018	View report
	No Evidence for Triplosensitivity		10/25/2018	View report