[description of familial occurrence of combined partial 17, 20-desmolase and 17alpha-hydroxylase deficiency in phenotypically normal normotensive women who presented with primary infertility, anovulation and persistent cervical dysmucorrhea ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE