BRDT, bromodomain testis associated, 676

N. diseases: 17; N. variants: 3
Disease: SPERMATOGENIC FAILURE 21 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4539991
Disease: SPERMATOGENIC FAILURE 21
SPERMATOGENIC FAILURE 21 		0.300 GeneticVariation disease UNIPROT Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa. 28199965 2017