Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Uniparental disomy, paternal, chromosome 14
0.020 Biomarker disease BEFREE Consistent with this, paternal uniparental disomy 14 (upd(14)pat), and epimutations (hypermethylations) and microdeletions affecting the IG-DMR and/or the MEG3-DMR of maternal origin, result in a unique phenotype associated with characteristic face, a small bell-shaped thorax with coat-hanger appearance of the ribs, abdominal wall defects, placentomegaly and polyhydramnios. 26377239 2016
Uniparental disomy, paternal, chromosome 14
0.020 GeneticVariation disease BEFREE Paternal uniparental disomy 14 (UPD(14)pat) results in a unique constellation of clinical features, and a similar phenotypic constellation is also caused by microdeletions involving the DLK1-MEG3 intergenic differentially methylated region (IG-DMR) and/or the MEG3-DMR and by epimutations (hypermethylations) affecting the DMRs. 22353941 2012