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inherited hemoglobinopathy

Disease Summary
Associated Targets (56)
Tbio

40

Tclin

11

Tchem

5


Mondo Description An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.
Mondo Term and Equivalent IDs
MONDO:0019050:  inherited hemoglobinopathy
COHD:432868: 
GARD:0012455: 
MESH:D006453: 
NCIT:C3092: 
Orphanet:68364: 
SCTID:427306008: 
UMLS:C0019045: 
UMLS:C1960031: