Human genes for biotinidase deficiency
Biotinidase deficiency [DOID:856]
A multiple carboxylase deficiency that involves a deficiency in biotinidase as the body is not able to use biotin and results in biotin deficiency, and has_material_basis_in homozygous or compound heterozygous mutation in the BTD gene on chromosome 3p25.
Synonyms: biotinidase deficiency, DOID:856, biotinidase deficiencies, BTD deficiency, Juvenile-onset multiple carboxylase deficiency ...
Linkouts: OMIM