A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
ID
http://purl.bioontology.org/ontology/MESH/D006453
altLabel
Hemoglobinopathy
AN
do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available
AQL
BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui
C0019045
DC
1
definition
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.