Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
0.010 GeneticVariation BEFREE HLA-DRB1*04 alleles in Japanese rheumatoid arthritis patients with AA amyloidosis. 17086601

2006

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0159060
Disease: Abnormal bowel sounds
Abnormal bowel sounds
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
Abnormal cardiac ventricular function
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
Abnormal liver parenchyma morphology
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0392188
Disease: Abnormal rapid eye movement sleep
Abnormal rapid eye movement sleep
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
Abnormal reproductive system morphology
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0149772
Disease: Abnormal salivary gland morphology
Abnormal salivary gland morphology
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C4023166
Disease: Abnormality of T cell physiology
Abnormality of T cell physiology
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C4021794
Disease: Abnormality of the adrenal glands
Abnormality of the adrenal glands
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
Abnormality of the gastrointestinal tract
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C4025854
Disease: Abnormality of the nasal mucosa
Abnormality of the nasal mucosa
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C4025698
Disease: Abnormality of the peritoneum
Abnormality of the peritoneum
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
0.100 Biomarker HPO

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C1321756
Disease: Achalasia
Achalasia
0.020 GeneticVariation BEFREE These results confirm the association between achalasia and HLA-DQ1 allele and suggest that TNFa11 is a marker for a protective allele for the disease, present on the B7-DRB1*1501 (7.1) ancestral haplotype in our population. 11019915

2000

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C1321756
Disease: Achalasia
Achalasia
0.020 Biomarker BEFREE Significant increases in the frequencies of alleles DRB1*14:54 and DQB1*05:03 and the extended haplotypes DRB1*14:54-DQB1*05:03 and DRB1*11:01-DQB1*03:01, even after Bonferroni correction (pC<0.05), were found in the achalasia group compared to those in the controls. 30092016

2018

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
0.010 GeneticVariation BEFREE Correlations between HLA-A, HLA-B and HLA-DRB1 allele polymorphisms and childhood susceptibility to acquired aplastic anemia. 22572536

2012

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia
0.010 GeneticVariation BEFREE A rare FVIII variant (E2004K) was found in one patient with acquired haemophilia after massive transfusion; the 2004 K allele was predicted to be presented on the patient's HLA-DRB1*0101. 20054547

2010

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
0.010 GeneticVariation BEFREE To evaluate the influence of HLA-DRB1 polymorphism in KS susceptibility among HHV-8 infected AIDS patients. 15075536

2004

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0406217
Disease: Actinic prurigo
Actinic prurigo
0.040 AlteredExpression BEFREE Furthermore, it has been shown that HLA-DR4 and DRB1*0407, even in association with polymorphic light eruption (PLE), are insufficient for the expression of the AP phenotype. 11722460

2001

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0406217
Disease: Actinic prurigo
Actinic prurigo
0.040 GeneticVariation BEFREE Allele-specific oligonucleotide DR4 subtyping showed that 80.7% of HLA-DR4+ patients with AP were also positive for the DRB1*0407 allele. 9204058

1997

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0406217
Disease: Actinic prurigo
Actinic prurigo
0.040 Biomarker BEFREE In conclusion, HLA-DRB1*03:01 was associated with AP in Singaporean Chinese patients. 26787110

2016

Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0406217
Disease: Actinic prurigo
Actinic prurigo
0.040 GeneticVariation BEFREE HLA typing subsequently confirmed the strong association (90%) between AP and the DR4 allele, in particular with the rare subtype DRB1*0407 which was present in 60% of these patients.No HLA association was found in PLE. 10233214

1999