TP63, tumor protein p63, 8626

N. diseases: 816; N. variants: 64
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 GeneticVariation disease GWASCAT Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. 28054174 2017
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 SusceptibilityMutation disease ORPHANET Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate. 21567929 2011
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 GeneticVariation disease BEFREE Ankyloblepharon-ectodermal defect-cleft lip and/or palate (AEC) is a rare genetic disorder due to mutations in the TP63 gene. 19676058 2009
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 SusceptibilityMutation disease ORPHANET A mutation of the p63 gene in non-syndromic cleft lip. 16740912 2006
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 GeneticVariation disease BEFREE A mutation of the p63 gene in non-syndromic cleft lip. 16740912 2006
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 GeneticVariation disease LHGDN A mutation of the p63 gene in non-syndromic cleft lip. 16740912 2006
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 Biomarker disease CTD_human Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients. 16688749 2006
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 Biomarker disease HPO
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.720 Biomarker disease GENOMICS_ENGLAND