Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0678202
Disease: Regional enteritis
Regional enteritis
0.100 GeneticVariation disease CLINVAR De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease. 28126021 2017
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.100 GeneticVariation disease GWASDB Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis. 24837172 2015
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
0.100 GeneticVariation phenotype GWASDB Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341 2012
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
0.100 GeneticVariation phenotype GWASCAT Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341 2012
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.100 GeneticVariation disease GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147 2010
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.030 AlteredExpression disease BEFREE Elevated level of HSPA1L mRNA correlates with graft-versus-host disease. 25680846 2015
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.030 Biomarker disease LHGDN The HSP-70/Hom rs2075800 G allele frequency was higher in the sarcoid-uveitis group than in both the sarcoid-non-uveitis and control groups (83% vs. 71%, OR = 2.00, P(c) = 0.01; and 83% vs. 66%, OR = 2.45, P(c) = 0.00005, respectively). 17591867 2007
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.030 GeneticVariation disease BEFREE A strong association was found between HSP-70/Hom rs2075800 G and uveitis in patients with sarcoidosis. 17591867 2007
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.030 GeneticVariation disease LHGDN HSP70-hom gene polymorphism as a prognostic marker of graft-versus-host disease. 17060867 2006
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.030 GeneticVariation disease BEFREE HSP70-hom gene single nucleotide (+2763 G/A and +2437 C/T) polymorphisms in sarcoidosis. 16611259 2006
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.030 GeneticVariation disease BEFREE In the present study, HSP70-hom polymorphism (+2763 G/A) was analyzed in the patients and donors of allogeneic HSCT in relation to transplantation outcome, susceptibility for generation of severe toxic lesions, and acute (a) graft-versus-host disease (GVHD). 15818324 2005
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.030 GeneticVariation disease BEFREE On the other hand, HSP70-hom locus analysis showed significantly increased frequency of A allele in the whole group of SpA (pC<0.05, OR=3.4), as well as in the groups with AS (pC<0.05, OR=5.6) and with uSpA (pC<0.05, OR=3.1), when compared with healthy controls. 11779758 2002
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.030 GeneticVariation disease BEFREE HSP70-1, HSP70-2 and HSP70-hom genotypes were analyzed by PCR-RFLP in patients with AS and in healthy controls. 9583810 1998
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.030 GeneticVariation disease BEFREE We screened the TNFA, TNFB, HSP70-1 and Hum70t genes around the class III region, as well as the HLA-DMA and -DMB genes in the class II region, for genetic polymorphism in sarcoidosis. 9349405 1997
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.030 GeneticVariation disease BEFREE The results indicated that the HSP70-Hom polymorphic variation is not connected independently to the different pathogenesis of AS and ReA, as no statistically significant differences between the patient groups and/or controls could be found. 9098422 1994
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.020 AlteredExpression disease BEFREE In the skin biopsies, HSPA1L mRNA expression was lower in patients with severe aGVHD (grades II-III) when compared to those with none or low grade aGVHD (grades 0-I) and normal controls. 25680846 2015
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 GeneticVariation disease BEFREE Our findings confirm the role of at-risk haplotype across the HSP70-hom/VEGF gene cluster in determining susceptibility to PCa. 20096741 2010
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 GeneticVariation disease BEFREE Our findings confirm the role of at-risk haplotype across the HSP70-hom/VEGF gene cluster in determining susceptibility to PCa. 20096741 2010
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation group BEFREE Since some factors may influence tumor progression rather than initiation, we also examined the relationship between the HSP70-hom polymorphism and the clinical characteristics of the malignancy at the time of diagnosis. 17578680 2008
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 GeneticVariation disease BEFREE Given the role of the molecular chaperone HSP70 in the regulation of the androgen receptor (AR) transactivation function, we first chose to explore the association between the HSP70-hom functional genetic variant (+2437 T > C) and prostate cancer risk by genotyping DNA samples from 101 unselected PCa patients and 105 healthy men. 17578680 2008
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 GeneticVariation disease BEFREE Given the role of the molecular chaperone HSP70 in the regulation of the androgen receptor (AR) transactivation function, we first chose to explore the association between the HSP70-hom functional genetic variant (+2437 T > C) and prostate cancer risk by genotyping DNA samples from 101 unselected PCa patients and 105 healthy men. 17578680 2008
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.020 GeneticVariation disease BEFREE HSP70-hom gene polymorphism in allogeneic hematopoietic stem-cell transplant recipients correlates with the development of acute graft-versus-host disease. 15818324 2005
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation group BEFREE The authors designed a case-controlled study to investigate the potential association of the polymorphisms of TNF-alpha and of hsp70-2 and hsp70-hom genes with malignant tumors. 9338474 1997
CUI: C0740391
Disease: Middle Cerebral Artery Occlusion
Middle Cerebral Artery Occlusion
0.010 GeneticVariation disease BEFREE To investigate the effect of HSP70-hom+2437 single nucleotide polymorphisms (SNPs) on hypoxia and ischemia condition, we constructed the neuronal hypoxic injury model and the rat middle cerebral artery occlusion (MCAO) model to compare the inhibition rate of neurons and detect the infarct volume as well as the expression of related apoptotic proteins in order to explore the possible mechanisms. 31170438 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 GeneticVariation group BEFREE We carried out a case-control study among 367 coke oven workers in northwest China, focused on three common HSP70 polymorphisms (HSP70-1 G190C, HSP70-2 A1267G and HSP70-hom T2437C), and evaluated the association of HSP70 gene polymorphisms with work sites for high risk of hypertension. 30217924 2018