Human genes for molybdenum cofactor deficiency type A
Molybdenum cofactor deficiency type A [DOID:0111164]
A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21.
Synonyms: molybdenum cofactor deficiency type A, DOID:0111164, molybdenum cofactor deficiency type As, MOCOD type A, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A ...