Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 GeneticVariation disease BEFREE All CM cases showed absent (<10%) p57 IHC in chorionic villi. 30394942 2020
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Abnormal chorionic villi were seen in all cases with histomorphological and/or p57 immunohistochemical features simulating either partial or complete mole. 30952972 2019
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 GeneticVariation disease BEFREE We compared the allele zygosity ratio in 11 nonmolar donor egg POC, 5 dispermic (heterozygous) CHM and 31 monospermic (homozygous) CHM, without knowledge of the use of a donor egg, the histologic findings, or results of p57 immunohistochemical staining. 28463912 2018
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Immunohistochemistry p57 demonstrated negative staining in the villous stromal and cytotrophoblastic cells, supporting the diagnosis of CHM. 28800576 2017
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Detailed histomorphological review along with p57 IHC was carried out in 28 diagnosed cases (23 CM, 4 PM and 1 molar pregnancy not categorized) and 25 controls of four normal placentas and 21 POC (8 non-hydropic and 13 HA). 28574027 2017
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE In a prospective series of 1024 products of conception specimens subjected to immunohistochemical analysis of p57 expression and molecular genotyping with short tandem-repeat markers, 288 CHMs were diagnosed, of which 126 were genotyped, including 16 invasive CHMs. 26535984 2016
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 GeneticVariation disease BEFREE Polymer-based immunohistochemical staining of p57(kip2) (paternally imprinted gene, expressed from maternal allele) is a very effective method that can be used to differentiate androgenetic complete mole from partial mole and hydropic abortion. 26161420 2015
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE Of the 14 androgenetic/biparental mosaics with discordant p57 expression, 6 were uniformly mosaic and 8 had a p57-negative androgenetic molar component. p57 expression is highly correlated with genotyping, serves as a reliable marker for diagnosis of complete hydatidiform moles, and identifies androgenetic cell lines in mosaic conceptions. 23887308 2014
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE Recognition of their distinctive p57 expression patterns and genotyping results can prevent misclassification as typical CHMs, PHMs, or nonmolar specimens. 23370656 2013
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Pathological review and genotyping of other molar pregnancies in these cases showed them to be typical CHM with negative p57(KIP2) immunostaining of the cytotrophoblast cells and villous stroma and to be diploid but biparental, confirming a diagnosis of familial recurrent hydatidiform mole (FRHM). 23125094 2013
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Correct classification of all cases combined ranged from 51% to 75% by morphology and 70% to 80% with p57, with statistically significantly better performance of faculty only in round 2 (P-values of 0.69, <0.01, and 0.15 for rounds 1 to 3, respectively). p57 immunostaining significantly improved recognition of CHMs (P<0.01) and had high reproducibility (κ=0.93 to 0.96) but had no impact on distinction of PHMs and NMs. 22992698 2012
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Cases were classified by 3 gynecologic pathologists on the basis of H&E slides (masked to p57 immunostaining and genotyping results) into 1 of 3 categories (CHM, PHM, or NM) during 2 diagnostic rounds; a third round incorporating p57 immunostaining results was also conducted. 22245958 2012
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 GeneticVariation disease BEFREE A case of complete hydatidiform mole in a perimenopausal woman with diagnostic usefulness of p57(kip2) immunohistochemistry and HER2 fluorescent in situ hybridization. 22197173 2012
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE Although p57 immunostaining alone can identify CHMs, which lack p57 expression because of the lack of maternal DNA, this analysis cannot distinguish PHMs from nonmolar specimens as both express p57 because of the presence of maternal DNA. 21293291 2011
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Twenty cases of CHM with negative p57(KIP2) immunostaining were also analyzed by genotyping and indicated the absence of maternal contribution and the homozygosity for a single paternal allele in concordance with the androgenetic and monospermic origin of CHM in these cases. 21767919 2011
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE These data suggest that the combination of p57 and FISH seems to be the best ancillary testing strategy to aid pathologists in the appropriate identification of CM, PM, and HA in POC specimens. 20093228 2010
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE Specimens with morphologic features suggestive of CHM yet retaining p57 expression should be subjected to molecular genotyping to establish a definitive diagnosis because misclassification as PHM underestimates the risk of persistent gestational trophoblastic disease. 19542869 2009
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Multiplex short tandem repeat DNA analysis confirms the accuracy of p57(KIP2) immunostaining in the diagnosis of complete hydatidiform mole. 16949913 2006
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE In addition, p57(KIP2) staining has the advantage of differentiating hydropic abortuses from CMs, a distinction not made by ploidy analysis. p57(KIP2) staining can be used in concert with ploidy studies to refine the diagnosis of early molar pregnancies. 15754295 2005
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Immunostaining for p57(KIP2) fails to discriminate between gestational trophoblastic tumours that have arisen from complete hydatidiform moles and those that have originated from other types of pregnancy. 15279631 2004
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 Biomarker disease BEFREE Complementary use of ploidy analysis and p57KIP2 status can now help to distinguish a diploid hydropic miscarriage (p57KIP2-positive), diploid complete mole (p57KIP2-negative) and triploid partial mole (p57KIP2-positive). 14511255 2003
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles. 12471053 2002
CUI: C0678213
Disease: Complete hydatidiform mole
Complete hydatidiform mole
0.100 AlteredExpression disease BEFREE In contrast, p57KIP2 expression in cytotrophoblast and villous mesenchyme was absent or markedly decreased in 58 of 59 complete hydatidiform moles. 11688455 2001