autosomal dominant beta thalassemia

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Summary

Literature (0)

DOID:0080770 - autosomal dominant beta thalassemia

Disease Ontology Definition:A beta thalassemia that has_material_basis_in one dominantly inherited mutated HBB gene and signs and symptoms of beta-thalassemia major or beta-thalassemia intermedia.

Synonyms: inclusion body beta-thalassemia

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:603902 - BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE

MIM:603902 - BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), beta thalassemia (is_a)