Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225197
Disease: PREIMPLANTATION EMBRYONIC LETHALITY 1
PREIMPLANTATION EMBRYONIC LETHALITY 1 		0.600 GeneticVariation disease UNIPROT TLE6 mutation causes the earliest known human embryonic lethality. 26537248 2015
CUI: C4225197
Disease: PREIMPLANTATION EMBRYONIC LETHALITY 1
PREIMPLANTATION EMBRYONIC LETHALITY 1 		0.600 Biomarker disease CTD_human
CUI: C4225197
Disease: PREIMPLANTATION EMBRYONIC LETHALITY 1
PREIMPLANTATION EMBRYONIC LETHALITY 1 		0.600 CausalMutation disease CLINVAR
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.100 GeneticVariation disease GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
CUI: C0021361
Disease: Female infertility
Female infertility 		0.100 Biomarker phenotype HPO
CUI: C0021361
Disease: Female infertility
Female infertility 		0.100 CausalMutation phenotype CLINVAR
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms 		0.010 AlteredExpression group LHGDN Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. 18551179 2008
CUI: C0017185
Disease: Gastrointestinal Neoplasms
Gastrointestinal Neoplasms 		0.010 Biomarker group BEFREE Tle6-like;TLE6D directly interact with the gastrointestinal tumor suppressor RUNX3 and antagonize RUNX3 target transactivation. 18551179 2008
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 Biomarker phenotype BEFREE Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. 18551179 2008