Supplementary Tables.pdf

<b>Table S1</b><b> </b><b>Distribution of phenotypes within the subtypes. </b>Values are presented as numbers with percentages in brackets. In the total cohort, from 258 women data was missing to determine the phenotype. In the subset NIH criteria, from 16 women data was missing to determine the phenotype. Abbreviations: OD, ovulatory dysfunction; PCOM, polycystic ovarian morphology; HA, hyperandrogenism. Phenotype A: OD +HA +PCOM, phenotype B: OD + HA, phenotype C: HA + PCOM, and phenotype D: OD +PCOM. <b>Table S2</b> <b>Comparison between classic NIH subset and non-NIH subset from the total cohort across the three subtypes. </b>Values are presented as numbers with percentages in brackets. Samples were stratified in the ‘Classic NIH’ and ‘non-NIH Rotterdam’ groups based on the clustering analysis from the total cohort. Phenotype A: OD +HA +PCOM, phenotype B: OD + HA, phenotype C: HA + PCOM, and phenotype D: OD +PCOM. Chi-squared test was performed to test for significance.