HBB, hemoglobin subunit beta, 3043

N. diseases: 272; N. variants: 188
Disease: Beta Thalassemia, Dominant Inclusion Body Type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 CausalMutation disease CLINVAR
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 Biomarker disease CTD_human
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 GeneticVariation disease CLINVAR
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 Biomarker disease GENOMICS_ENGLAND Significant haemoglobinopathies: guidelines for screening and diagnosis. 20067565 2010
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		0.700 GermlineCausalMutation disease ORPHANET Hemoglobinopathies: clinical manifestations, diagnosis, and treatment. 21886666 2011