LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1832244
Disease: CARDIOMYOPATHY, DILATED, 1C (disorder)
CARDIOMYOPATHY, DILATED, 1C (disorder) 		0.900 CausalMutation disease CLINVAR
CUI: C1832244
Disease: CARDIOMYOPATHY, DILATED, 1C (disorder)
CARDIOMYOPATHY, DILATED, 1C (disorder) 		0.900 Biomarker disease MGD
CUI: C1832244
Disease: CARDIOMYOPATHY, DILATED, 1C (disorder)
CARDIOMYOPATHY, DILATED, 1C (disorder) 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C1832244
Disease: CARDIOMYOPATHY, DILATED, 1C (disorder)
CARDIOMYOPATHY, DILATED, 1C (disorder) 		0.900 Biomarker disease CTD_human
CUI: C1832244
Disease: CARDIOMYOPATHY, DILATED, 1C (disorder)
CARDIOMYOPATHY, DILATED, 1C (disorder) 		0.900 Biomarker disease GENOMICS_ENGLAND
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.410 Biomarker group GENOMICS_ENGLAND
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.410 Biomarker group HPO
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 CausalMutation disease CLINVAR
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 Biomarker disease HPO
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		0.410 Biomarker disease CTD_human
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4 		0.400 Biomarker disease GENOMICS_ENGLAND
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4 		0.400 CausalMutation disease CLINVAR
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.330 Biomarker group HPO
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.330 Biomarker group MGD
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.310 SusceptibilityMutation disease ORPHANET
CUI: C3152137
Disease: LEFT VENTRICULAR NONCOMPACTION 3
LEFT VENTRICULAR NONCOMPACTION 3 		0.200 Biomarker disease MGD
CUI: C4225414
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24 		0.200 Biomarker disease MGD
CUI: C0026848
Disease: Myopathy
Myopathy 		0.110 Biomarker group HPO
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker disease HPO
CUI: C0018794
Disease: Heart Block
Heart Block 		0.100 Biomarker disease HPO
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.100 Biomarker disease HPO
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		0.100 Biomarker disease HPO
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		0.100 Biomarker disease HPO
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop 		0.100 Biomarker phenotype HPO
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		0.100 Biomarker phenotype HPO