BRDT, bromodomain testis associated, 676

N. diseases: 17; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4022698
Disease: Acephalic spermatozoa
Acephalic spermatozoa
0.110 GeneticVariation disease BEFREE Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa. 28199965 2017
CUI: C4022698
Disease: Acephalic spermatozoa
Acephalic spermatozoa
0.110 Biomarker disease HPO