Methylmalonic aciduria, cblD type, variant 2 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C1848554
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Genes

1 genes associated with the Methylmalonic aciduria, cblD type, variant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria