hemoglobin M disease (Q55787691)
human disease
Language:
other details
aliases M hemoglobinopathy
 inherited methemoglobinemia type 2
 generalized reductase deficiency
description human disease

External Links
(P486) C581942
(P1550) 330041
(P2892) C3665425
(P4229) D74.0
(P5270) MONDO_0018023