| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A multiple carboxylase deficiency that involves a deficiency in biotinidase. (Human Disease Ontology, DOID_856) |
| External Link | http://www.omim.org/entry/253260 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the biotinidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| BTD | biotinidase |
