NUDT10, nudix hydrolase 10, 170685

N. diseases: 23; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Addison's disease due to autoimmunity
0.070 Biomarker disease BEFREE Stage 1 (increased plasma renin) for patients with APS-1 and Stage 2 (no response of cortisol to ACTH-test) for patients with APS-2/APS-4 were established as the points of no return in the progression to AAD. 30608902 2019
Autoimmune Primary Adrenal Insufficiency
0.070 Biomarker disease BEFREE Stage 1 (increased plasma renin) for patients with APS-1 and Stage 2 (no response of cortisol to ACTH-test) for patients with APS-2/APS-4 were established as the points of no return in the progression to AAD. 30608902 2019
Addison's disease due to autoimmunity
0.070 GeneticVariation disease BEFREE The strength of association in patients with isolated AAD appears to be weak or nonexistent compared to that in APS2. 21521299 2011
Autoimmune Primary Adrenal Insufficiency
0.070 GeneticVariation disease BEFREE The strength of association in patients with isolated AAD appears to be weak or nonexistent compared to that in APS2. 21521299 2011
Addison's disease due to autoimmunity
0.070 Biomarker disease BEFREE We conclude that polymorphisms in the AIRE gene are not associated with AAD and APS II. 18200029 2008
Autoimmune Primary Adrenal Insufficiency
0.070 Biomarker disease BEFREE We conclude that polymorphisms in the AIRE gene are not associated with AAD and APS II. 18200029 2008
Addison's disease due to autoimmunity
0.070 Biomarker disease BEFREE APS2, which occurs at a much higher frequency, is classically defined as the coexistence of autoimmune Addison's disease, autoimmune thyroid disease, and/or type 1 diabetes. 17911431 2007
Autoimmune Primary Adrenal Insufficiency
0.070 Biomarker disease BEFREE APS2, which occurs at a much higher frequency, is classically defined as the coexistence of autoimmune Addison's disease, autoimmune thyroid disease, and/or type 1 diabetes. 17911431 2007
Addison's disease due to autoimmunity
0.070 Biomarker disease BEFREE We determined the HLA-DR and HLA-DQA1 association in 112 unrelated patients with APS II (n = 29), APS III (n = 83) and 184 unrelated patients with single-component diseases without further manifestations of APS: Graves' disease (n = 70), Hashimoto's thyroiditis (n = 53), autoimmune Addison's disease (n = 15), vitiligo (n = 16) and alopecia (n = 30), and 72 healthy controls - German Caucasians - to identify possible predisposing and protective HLA class II alleles in APS. 12734793 2003
Autoimmune Primary Adrenal Insufficiency
0.070 Biomarker disease BEFREE We determined the HLA-DR and HLA-DQA1 association in 112 unrelated patients with APS II (n = 29), APS III (n = 83) and 184 unrelated patients with single-component diseases without further manifestations of APS: Graves' disease (n = 70), Hashimoto's thyroiditis (n = 53), autoimmune Addison's disease (n = 15), vitiligo (n = 16) and alopecia (n = 30), and 72 healthy controls - German Caucasians - to identify possible predisposing and protective HLA class II alleles in APS. 12734793 2003
Addison's disease due to autoimmunity
0.070 Biomarker disease BEFREE There was an association of the G allele at CTLA-4A/G in AAD subjects (P = 0.008 vs. controls), which was stronger in subjects with AAD as a component of APS2 than in subjects with isolated AAD. 10690877 2000
Addison's disease due to autoimmunity
0.070 GeneticVariation disease BEFREE Autoimmune Addison's disease (autoimmune adrenalitis) often occurs in autoimmune polyendocrinopathy syndromes APS1 (APECED) and APS2. 10920386 2000
Autoimmune Primary Adrenal Insufficiency
0.070 Biomarker disease BEFREE There was an association of the G allele at CTLA-4A/G in AAD subjects (P = 0.008 vs. controls), which was stronger in subjects with AAD as a component of APS2 than in subjects with isolated AAD. 10690877 2000
Autoimmune Primary Adrenal Insufficiency
0.070 GeneticVariation disease BEFREE Autoimmune Addison's disease (autoimmune adrenalitis) often occurs in autoimmune polyendocrinopathy syndromes APS1 (APECED) and APS2. 10920386 2000
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 GeneticVariation disease BEFREE She was diagnosed as autoimmune polyglandular syndrome (APS) (Hashimoto thyroiditis and possible primary adrenal insufficiency) as well as primary hypoparathyroidism and Sjögren's syndrome, which are very rarely complicated in APS-2. 31133546 2019
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 GeneticVariation disease BEFREE Dividing the APS collective into those with Addison's disease (APS type II) and those without Addison's disease but including type 1 diabetes and AITD (APS type III) demonstrated DR3-DQ2/DRB1*04:01-DQ8 as a susceptibility genotype in APS III (Pc<.001), whereas the DR3-DQ2/DRB1*04:04-DQ8 genotype correlated with APS II (Pc<.001). 24187405 2014
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 Biomarker disease BEFREE The two major autoimmune polyendocrine syndromes, (type1-type2/APS-1 and APS-2), both have Addison's disease as a prominent component. 24055063 2014
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 Biomarker disease BEFREE No significant differences were reported for the frequency of DR3-DQ2 and DR4-DQ8 haplotypes in a recent study of one of the largest cohorts worldwide of patients with isolated Addison's disease compared to patients with APS II. 12734793 2003
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 GeneticVariation disease BEFREE Human leukocyte antigen (HLA)-DRB1 and -DQB1 alleles were analyzed using a PCR-based sequence-specific priming technique in 16 patients with autoimmune polyglandular syndrome type I (APS-I), 31 patients with APS-II, and 110 patients with component diseases of APS-II, including 9 patients with isolated Addison's disease, 43 patients with Hashimoto's thyroiditis, 22 patients with Graves' disease, and 36 patients with vitiligo. 8675578 1996
CUI: C0001403
Disease: Addison Disease
Addison Disease
0.060 Biomarker disease BEFREE Our results show that patients with Addison's disease in association with APS2 or Addison's disease as an isolated form share highly similar MHC class II and class III alleles. 7860358 1994
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
0.050 GeneticVariation group BEFREE She was diagnosed as autoimmune polyglandular syndrome (APS) (Hashimoto thyroiditis and possible primary adrenal insufficiency) as well as primary hypoparathyroidism and Sjögren's syndrome, which are very rarely complicated in APS-2. 31133546 2019
Polyglandular Type I Autoimmune Syndrome
0.050 Biomarker disease BEFREE Results The cumulative risk (CR) of developing AAD was higher in APS-1 patients (94.2%) compared to patients with APS-2/APS-4 (38.7%). 30608902 2019
Diabetes Mellitus, Insulin-Dependent
0.050 GeneticVariation disease BEFREE Dividing the APS collective into those with Addison's disease (APS type II) and those without Addison's disease but including type 1 diabetes and AITD (APS type III) demonstrated DR3-DQ2/DRB1*04:01-DQ8 as a susceptibility genotype in APS III (Pc<.001), whereas the DR3-DQ2/DRB1*04:04-DQ8 genotype correlated with APS II (Pc<.001). 24187405 2014
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
0.050 GeneticVariation group BEFREE Dividing the APS collective into those with Addison's disease (APS type II) and those without Addison's disease but including type 1 diabetes and AITD (APS type III) demonstrated DR3-DQ2/DRB1*04:01-DQ8 as a susceptibility genotype in APS III (Pc<.001), whereas the DR3-DQ2/DRB1*04:04-DQ8 genotype correlated with APS II (Pc<.001). 24187405 2014
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
Polyendocrinopathies, Autoimmune
0.050 Biomarker group BEFREE The sizes of thrombi were significantly smaller in the C6(-/-) mice injected with IgG-APS1, IgG-APS2 or IgM-APS (p < 0.001), compared to their C6(+/+) counterparts showing an important abrogation of thrombus formation in mice lacking C6. 22933620 2012