Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia
0.010 GeneticVariation disease BEFREE beta thalassemia (beta thal) in DBA/2J mice is a consequence of the spontaneous and complete deletion of the beta major globin gene. 8562946 1996
CUI: C3841475
Disease: beta^+^ Thalassemia
beta^+^ Thalassemia
0.010 GeneticVariation disease BEFREE beta thalassemia (beta thal) in DBA/2J mice is a consequence of the spontaneous and complete deletion of the beta major globin gene. 8562946 1996
CUI: C0949116
Disease: Congenital hypoplastic anemia
Congenital hypoplastic anemia
0.010 GeneticVariation disease BEFREE A 7 year old girl is described with congenital hypoplastic anaemia (Diamond-Blackfan anaemia, DBA) and an apparently balanced reciprocal translocation, 46,XX,t(X;19)(p21;q13). 9321770 1997
CUI: C0003864
Disease: Arthritis
Arthritis
0.100 Biomarker disease BEFREE To find an "unlimited" source of antigenic material (aggrecan) for arthritis induction in BALB/c mice; to analyze the specificities of immune reactions to aggrecan and type II collagen in 2 arthritis-susceptible murine strains, BALB/c mice for proteoglycan (aggrecan)-induced arthritis and DBA/1j mice for collagen-induced arthritis; to compare the histopathologic features of arthritis induced by purified aggrecans or total extracts of osteoarthritic (OA) cartilage; and to determine arthritis susceptibility in various BALB/c colonies. 9627010 1998
CUI: C0003864
Disease: Arthritis
Arthritis
0.100 GeneticVariation disease BEFREE Localization of non-Mhc collagen-induced arthritis susceptibility loci in DBA/1j mice. 10051620 1999
CUI: C0007370
Disease: Catalepsy
Catalepsy
0.010 Biomarker disease BEFREE Detection and mapping of quantitative trait loci for haloperidol-induced catalepsy in a C57BL/6J x DBA/2J F2 intercross. 10765558 1999
CUI: C0036572
Disease: Seizures
Seizures
0.040 Biomarker phenotype BEFREE This article describes the identification of SLC19A3, a gene encoding a novel solute transporter, and establishes murine SLC19A3 as a candidate gene for seizures in the DBA/2J mouse. 11136550 2000
CUI: C0036572
Disease: Seizures
Seizures
0.040 GeneticVariation phenotype BEFREE F2 mice derived from a C3H x DBA cross that were homozygous for the C3H variant of the alpha7 RFLP were more sensitive to nicotine-induced seizures than were F2 mice that were homozygous for the DBA RFLP. 10942032 2000
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 GeneticVariation disease BEFREE With respect to virernia, in two subjects with low titre of HBV DNA (< 100 MEq/ml), no variation was found in the YMDD motif, whereas in seven patients with high titre of HBV DBA (> 300 MEq/ml), five (71%) had variations in the YMDD motif. 11776105 2000
CUI: C2673892
Disease: Ductal plate malformation
Ductal plate malformation
0.010 AlteredExpression disease BEFREE DBA/2J (D2), CD-1, BALB/c and Mus mus castaneus (CAST), express the DPM. 10749984 2000
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.100 Biomarker disease BEFREE Despite the phenotypic similarity between the glaucoma in the DBA/2J mouse and human pigmentary glaucoma, the results of this study suggest that DNA sequence variants in the human TYRP1 gene are not associated with inherited pigmentary glaucoma in humans. 12011806 2002
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.040 Biomarker disease BEFREE DBA/2J (D2) mice develop a form of pigmentary glaucoma involving iris pigment dispersion (IPD) and iris stromal atrophy (ISA). 11743578 2002
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
0.010 Biomarker disease BEFREE In contrast, none of female CBA/J (H-2(k)), DBA/1J (H-2(q)), or SJL/J (H-2(s)) mice developed Graves' hyperthyroidism or anti-TSHR autoantibodies except SJL/J, which showed strong TBII activities. 11884447 2002
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 Biomarker disease BEFREE These tumors occur at much younger ages than in the general population, in patients who do not appear to have the usual risk factors, and have patterns that are characteristic to the syndrome, such as head and neck and gynecologic cancers in FA and DC, and osteogenic sarcomas in DBA. 12430621 2002
CUI: C0423319
Disease: Atrophic iris
Atrophic iris
0.010 GeneticVariation disease BEFREE Recently, a form of glaucoma associated with pigment dispersion and iris atrophy was identified in the DBA/2J mouse. 12011806 2002
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome
0.010 Biomarker disease BEFREE These tumors occur at much younger ages than in the general population, in patients who do not appear to have the usual risk factors, and have patterns that are characteristic to the syndrome, such as head and neck and gynecologic cancers in FA and DC, and osteogenic sarcomas in DBA. 12430621 2002
CUI: C0003864
Disease: Arthritis
Arthritis
0.100 Biomarker disease BEFREE To induce arthritis in mice, rYKL-39 (1, 10 or 50 g in Freund's incomplete adjuvant) was injected into the right footpad of mice from four different strains (BALB/c, DBA/1J, C57BL/6 and ICR). 12102470 2003
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 Biomarker disease BEFREE DBA/2J animals were 3-fold more sensitive to AFB(1)-induced HCC and significantly more sensitive to AFB(1) acute toxicity than were C57BL/6J animals. 12907637 2003
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
0.010 Biomarker group BEFREE To evaluate the genetic susceptibility to metabolic disorders induced by high fructose diet, we investigated the metabolic characteristics in 10 strains of inbred mice and found that they were separated into CBA and DBA groups according to the response to high fructose diet. 15123654 2004
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.040 Biomarker disease BEFREE We also observed that activated NF-kappaB and phosphorylated MAPK are increased in the iris/ciliary body of DBA/2J mice, suggesting that both signaling pathways may be involved in IL-18 mediated pathogenesis of pigmentary glaucoma in the eyes of DBA/2J mice. 15985430 2005
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.100 Biomarker disease BEFREE DBA/2J (D2) mice develop an age-related form of glaucoma. 16827931 2006
CUI: C0003864
Disease: Arthritis
Arthritis
0.100 Biomarker disease BEFREE MHC class II derived recombinant T cell receptor ligands protect DBA/1LacJ mice from collagen-induced arthritis. 18178865 2008
CUI: C0021400
Disease: Influenza
Influenza
0.040 Biomarker disease BEFREE To model host factors in the context of influenza virus infection, we determined the lethal dose of a highly pathogenic H5N1 virus (A/Hong Kong/213/03) in C57BL/6J and DBA/2J mice and identified genetic elements associated with survival after infection. 19706712 2009
CUI: C1260899
Disease: Anemia, Diamond-Blackfan
Anemia, Diamond-Blackfan
0.050 GeneticVariation disease BEFREE As RP mutations are yet to be identified in approximately 50% of DBA cases, it is likely that other yet to be identified genes involved in ribosomal biogenesis or other pathways may be responsible for DBA phenotype. 20655265 2010
CUI: C2676137
Disease: Diamond-Blackfan Anemia 1
Diamond-Blackfan Anemia 1
0.030 GeneticVariation disease BEFREE As RP mutations are yet to be identified in approximately 50% of DBA cases, it is likely that other yet to be identified genes involved in ribosomal biogenesis or other pathways may be responsible for DBA phenotype. 20655265 2010