TPI1, triosephosphate isomerase 1, 7167

N. diseases: 184; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE Clinical TPI deficiency is a rare autosomal recessive multi-system disorder characterised by non-spherocytic haemolytic anaemia, recurrent infections, cardiomyopathy, severe and fatal neuromuscular dysfunctions. 9850739 1998
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency. 29720471 2018
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE Triosephosphate isomerase (TPI) deficiency is a poorly understood disease characterized by hemolytic anemia, cardiomyopathy, neurologic dysfunction, and early death. 27031109 2016
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE We report the clinical, haematological and molecular characteristics of two triose phosphate isomerase deficient patients affected by haemolytic anaemia and neuromuscular impairment. 20374271 2010
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 GeneticVariation disease BEFREE The disease is caused exclusively by specific missense mutations affecting the TPI protein and clinically features hemolytic anemia, adult-onset neurological impairment, degeneration, and reduced longevity. 18458110 2008
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE Of the several well-established glycolytic enzyme deficiencies, triosephosphate isomerase (TPI) deficiency is the only one in which haemolytic anaemia is coupled with progressive, severe neurological disorder. 12023819 2002
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 Biomarker disease BEFREE Triosephosphate isomerase (TPI) deficiency is a fatal genetic disorder characterized by hemolytic anemia and neurological dysfunction. 31111503 2019
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.480 GeneticVariation disease BEFREE Mutations in the gene triosephosphate isomerase (TPI) lead to a severe multisystem condition that is characterized by hemolytic anemia, a weakened immune system, and significant neurologic symptoms such as seizures, distal neuropathy, and intellectual disability.No effective therapy is available. 31075491 2019
CUI: C0520572
Disease: Enzymopathy
Enzymopathy
0.330 GeneticVariation group BEFREE Biochemical studies demonstrate that mutation of this glycolytic enzyme gene does not result in a bioenergetic deficit, suggesting an alternate cause of enzymopathy associated with TPI impairment. 16980388 2006
CUI: C0520572
Disease: Enzymopathy
Enzymopathy
0.330 AlteredExpression group BEFREE Both parents and some other family members had moderately reduced erythrocyte TPI activity in accordance with the autosomal recessive mode of inheritance in this enzymopathy. 669702 1978
CUI: C0520572
Disease: Enzymopathy
Enzymopathy
0.330 Biomarker group BEFREE Triose phosphate isomerase (TPI) deficiency glycolytic enzymopathy is a progressive neurodegenerative condition that remains poorly understood. 18458110 2008
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.320 Biomarker disease BEFREE One of the most strongly nitrotyrosinated proteins in AD is the triosephosphate isomerase (TPI) enzyme which regulates glycolytic flow, and its efficiency decreased when it is nitrotyrosinated. 24614897 2014
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.320 Biomarker disease BEFREE To assess the safety, tolerability, and pharmacodynamics of the microtubule stabilizer TPI-287 (abeotaxane) in Alzheimer disease (AD) or the 4-repeat tauopathies (4RT) progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS). 31710340 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.320 Biomarker disease BEFREE <b>Objectives:</b> To explore the acceptability of telepresence robots in dementia care from the perspectives of people with dementia, family carers, and health professionals/trainees, and investigate the utility of a social presence assessment tool, the Modified-Temple Presence Inventory (Modified-TPI), for people with dementia. 30450924 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.320 GeneticVariation disease BEFREE More falls (3 in the placebo group vs 11 in the TPI-287 group) and a dose-related worsening of dementia symptoms (mean [SD] in the CDR plus NACC FTLD-SB [Clinical Dementia Rating scale sum of boxes with frontotemporal dementia measures], 0.5 [1.8] in the placebo group vs 0.7 [1.6] in the TPI-287 group; median difference, 1.5 [95% CI, 0-2.5]; P = .03) were seen in patients with 4RT. 31710340 2019
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases
0.310 AlteredExpression group BEFREE A 16-month-old girl of Spanish origin with chronic hemolytic anemia and severe neuromuscular disease was found to have markedly reduced triosephosphate isomerase (TPI) activity in her erythrocytes, leukocytes, and plateletes. 669702 1978
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.310 GeneticVariation disease BEFREE When we analyzed the genetic polymorphisms of the single nucleotide polymorphisms (SNPs) of their human orthologous genes in a Korean population, the promoter SNPs of CKB and TPI1 were weakly associated with schizophrenia. 22623148 2012
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.310 AlteredExpression disease BEFREE Antioxidant enzyme AOE372, ATP synthase subunit d (ATP5D), beta1,4-galactosyltransferase, cytosolic inorganic pyrophosphatase, glucose-regulated M(r) 58,000 protein, glutathione-S-transferase M4, prolyl 4-hydroxylase beta subunit, triosephosphate isomerase, and ubiquitin thiolesterase (UCHL1) were identified as being significantly overexpressed in lung adenocarcinomas. 12114434 2002
Triose phosphate isomerase deficiency
0.310 GeneticVariation disease BEFREE Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene. 20374271 2010
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.130 Biomarker disease BEFREE Biomarker guidance allows a more personalized allocation of patients for remote patient management in heart failure: results from the TIM-HF2 trial. 31129929 2019
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.130 Biomarker disease BEFREE Numerous second-generation telemedicine projects have emerged in Europe over the last ten years or are still under development for computer science heart failure, especially in Europe, such as SCAD, OSICAT, E-care, PRADO-INCADO, and TIM-HF2. 30551588 2018
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.130 Biomarker disease BEFREE The TIM-HF2 trial will provide important prospective data on the potential beneficial effect of telemedical monitoring and RPM on unplanned cardiovascular hospitalisations and mortality in HF patients. 30230666 2018
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia
0.110 AlteredExpression disease BEFREE A 16-month-old girl of Spanish origin with chronic hemolytic anemia and severe neuromuscular disease was found to have markedly reduced triosephosphate isomerase (TPI) activity in her erythrocytes, leukocytes, and plateletes. 669702 1978
CUI: C0017536
Disease: Giardiasis
Giardiasis
0.100 GeneticVariation disease BEFREE Giardia duodenalis isolates recovered from humans and dogs living in the same locality in a remote tea-growing community of northeast India were characterized at 3 different loci; the SSU-rDNA, elongation factor 1-alpha (ef1-alpha) and triose phosphate isomerase (tpi) gene. 15080083 2004
CUI: C0017536
Disease: Giardiasis
Giardiasis
0.100 Biomarker disease BEFREE Assemblage study for Giardia lamblia was performed using triose phosphate isomerase (TPI) as the target gene. 27934806 2016