Methylmalonic aciduria cblB type Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An organic acidemia that involves an accumulation of methylmalonic acid in the blood. (Human Disease Ontology, DOID_14749)
External Link http://www.omim.org/entry/251110
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Methylmalonic aciduria cblB type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type