Term Name: molybdenum cofactor deficiency type A
Synonyms: combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A, MOCOD type A, MOCODA, molybdenum cofactor deficiency complementation group A
Definition: A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS1 gene on chromosome 6p21.
Ontology: Human Disease [DOID:0111164]   ( DOID:0111164 )

Relationships
is a type of: molybdenum cofactor deficiency