Sickle Cell Disease Ontology Project Beta-Zero Thalassemia Mutation http://scdontology.h3abionet.org/ontology/SCDO_0002475 A mutation in the beta-globin gene, HBB, that results in absent beta globin synthesis. Term info curator note Request inclusion into relevant ontology dc:creator SCDO existence in other ontologies None Beta Null Mutation Term relations Subclass of: Beta Thalassemia Mutation Related from: has contributing genetic variation Hemoglobin Genotype S/Beta Zero Thalassaemia Beta Zero Thalassemia Please enable JavaScript to view the comments powered by Disqus.
