Hemoglobin H Disease
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by chronic hemolytic anemia.
Sickle Cell Disease Ontology Project
Term info
database cross reference
- NCIT:C95504
database cross reference
NCIT:C95504
definition source
http://bioportal.bioontology.org/ontologies/NCIT/?p=classes&conceptid=http%3A%2F%2Fncicb.nci.nih.gov%2Fxml%2Fowl%2FEVS%2FThesaurus.owl%23C95504
existence in other ontologies
Sufficient
Alpha-Thalassemia Intermedia, Haemoglobin H Disease, Hb H-Disease