Biotinidase Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A multiple carboxylase deficiency that involves a deficiency in biotinidase. (Human Disease Ontology, DOID_856)
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Genes

1 genes associated with the Biotinidase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BTD biotinidase