Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.240 Biomarker disease BEFREE Here we examined the role of splicing factors hnRNP A1/A1b and hnRNP A2/B1 in hepatocellular carcinoma (HCC). 24572810 2014
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.210 Biomarker disease BEFREE Therefore, we suggest that the increased expression and cytoplasmic localization of hnRNP A2/B1 can be used as a diagnostic biomarker to assess the risk of human liver cancer. 20604928 2010
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.210 Biomarker disease RGD Mitogenic insulin receptor-A is overexpressed in human hepatocellular carcinoma due to EGFR-mediated dysregulation of RNA splicing factors. 23633480 2013
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		0.200 Biomarker disease RGD Histochemical mapping of hnRNP A2/B1 in rat brain after ischemia-reperfusion insults. 20421594 2010
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		0.200 Biomarker disease RGD Proteomics analysis identifies molecular targets related to diabetes mellitus-associated bladder dysfunction. 18337374 2008
CUI: C0023903
Disease: Liver neoplasms
Liver neoplasms 		0.200 Biomarker group RGD Mitogenic insulin receptor-A is overexpressed in human hepatocellular carcinoma due to EGFR-mediated dysregulation of RNA splicing factors. 23633480 2013
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma 		0.200 Biomarker disease RGD Mitogenic insulin receptor-A is overexpressed in human hepatocellular carcinoma due to EGFR-mediated dysregulation of RNA splicing factors. 23633480 2013
CUI: C2676033
Disease: Hepatoblastoma Caused By Somatic Mutation
Hepatoblastoma Caused By Somatic Mutation 		0.200 Biomarker disease RGD Mitogenic insulin receptor-A is overexpressed in human hepatocellular carcinoma due to EGFR-mediated dysregulation of RNA splicing factors. 23633480 2013
CUI: C0026848
Disease: Myopathy
Myopathy 		0.120 Biomarker group BEFREE Ectopic expression of the disease-associated mutant form of hnRNPA2B1 or Hrb98DE in fly muscle resulted in progressive, age-dependent cytoplasmic inclusion pathology, as observed in humans with hnRNPA2B1-related myopathy. 26744327 2016
CUI: C0026848
Disease: Myopathy
Myopathy 		0.120 Biomarker group HPO
CUI: C0026848
Disease: Myopathy
Myopathy 		0.120 Biomarker group BEFREE Mutations in the genes encoding the heterogeneous nuclear ribonucleoproteins hnRNPA1 and hnRNPA2/B1 have been reported in a multisystem proteinopathy that includes amyotrophic lateral sclerosis (ALS) and inclusion body myopathy associated with Paget disease of the bone and frontotemporal dementia. 29131108 2017
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		0.120 Biomarker disease BEFREE Mutations in the genes encoding the heterogeneous nuclear ribonucleoproteins hnRNPA1 and hnRNPA2/B1 have been reported in a multisystem proteinopathy that includes amyotrophic lateral sclerosis (ALS) and inclusion body myopathy associated with Paget disease of the bone and frontotemporal dementia. 29131108 2017
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		0.120 Biomarker disease HPO
CUI: C0003537
Disease: Aphasia
Aphasia 		0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker disease HPO
CUI: C0015644
Disease: Muscular fasciculation
Muscular fasciculation 		0.100 Biomarker phenotype HPO
CUI: C0015695
Disease: Fatty Liver
Fatty Liver 		0.100 Biomarker disease HPO
CUI: C0016663
Disease: Pathological fracture
Pathological fracture 		0.100 Biomarker phenotype HPO
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.100 Biomarker disease HPO
CUI: C0019559
Disease: Hip joint pain
Hip joint pain 		0.100 Biomarker phenotype HPO
CUI: C0023015
Disease: Language Disorders
Language Disorders 		0.100 Biomarker group HPO
CUI: C0024003
Disease: Lordosis
Lordosis 		0.100 Biomarker phenotype HPO
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.100 Biomarker disease HPO
CUI: C0026884
Disease: Mutism
Mutism 		0.100 Biomarker phenotype HPO
CUI: C0027121
Disease: Myositis
Myositis 		0.100 Biomarker disease HPO