CYB5A methemoglobinemiamethemoglobinemia caused by mutation in CYB5Amethemoglobinemia type 4METAGisolated 17,20-lyase deficiency, Puremethemoglobinemia and ambiguous genitaliamethemoglobinemia due to deficiency of cytochrome B5methemoglobinemia due to deficiency of cytochrome B5, formerlymethemoglobinemia type IVmethemoglobinemia type IV, formerly
Definition
Any methemoglobinemia in which the cause of the disease is a mutation in the CYB5A gene.
Patient-Friendly Information
Comprehensive, easy-to-understand information about this condition