Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110031 - hemoglobin H disease

Disease Ontology Definition:An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other.

Synonyms: alpha thalassemia, haemoglobin H type, alpha thalassemia, hemoglobin H type, alpha-thalassemia intermedia, haemoglobin H disease, haemoglobin H disease, deletional, HBH, hemoglobin H disease, deletional

Xenbase Genes : hba1, hba2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013512 - hemoglobin H disease


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): alpha thalassemia (is_a)