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## Description Summarize the changes Fixes: #318 , #295 , #317 , #284. #322, #319, #308 ## Major Changes - Updating outdated "mental retardation" to "intellectual development disorder" in FRAXE (#318), FXS, & XMLR - AFF2 name change (#318 ) and incomplete list of HPO terms added - XLMR name change and disease ID change to XID and PHPX and overlap described - New mechanistic information for OPDM2 (#295) - Additional name added to NIID (#317) - Added benign motif to CANVAS - Handful of Motifs added to RFC1 (#322) - FTDALS1 pathogenic minimum brought down to 31 (intermediate brought down to 30) ## Minor Changes - FMR1 gene updated to fragile X messenger ribonucleoprotein 1 in FXS description - Added phenotype for premutation to FXTAS - Additional mechanism detail added to NIID - Added phenotype to CCHS ## Checklist - [x] All changes are well summarized - [ ] Check all tests pass - [ ] Check that the website preview looks good - [x] Update the STRchive version in `CITATION.cff`, format X.Y.Z. If any major changes, increment Y. If only minor changes, increment Z. If the breaking change (rare), increment X. - [ ] Ask someone to review this PR --------- Co-authored-by: Harriet Dashnow <h.dashnow@gmail.com> Co-authored-by: hdashnow <3794821+hdashnow@users.noreply.github.com> Co-authored-by: github-actions[bot] <41898282+github-actions[bot]@users.noreply.github.com>
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Name
Harriet Dashnow
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@hdashnow
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Description
Changing the phenotype nomenclature to reflect a move away from outdated terminology. Also added an incomplete list of HPO terms.