CYB5A

cytochrome b5 type A
OMIM: 613218
PanelMode of inheritanceDetails
1 panel
R-numbers: R146
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
46,XY underandrogenization with biochemistry similar to isolated 17,20-lyase deficiency, Methemoglobinemia, type I, 250790