Biotinidase Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A multiple carboxylase deficiency that involves a deficiency in biotinidase. (Human Disease Ontology, DOID_856)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D028921
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Genes

1 genes/proteins associated with the disease Biotinidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
BTD biotinidase 2.88009