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: 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
CUI: C0241005
Disease: Creatine phosphokinase serum increased
Creatine phosphokinase serum increased 		0.100 Biomarker phenotype HPO
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left 		0.100 Biomarker phenotype HPO
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		0.100 Biomarker phenotype HPO
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal 		0.100 Biomarker phenotype HPO
CUI: C0544966
Disease: Autophagic vaculoes (finding)
Autophagic vaculoes (finding) 		0.100 Biomarker phenotype HPO
CUI: C0553980
Disease: Endomyocardial Fibrosis
Endomyocardial Fibrosis 		0.100 Biomarker phenotype HPO
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		0.100 Biomarker group HPO
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C1280433
Disease: Lipoatrophy
Lipoatrophy 		0.100 Biomarker disease HPO
CUI: C1834536
Disease: Weakness of the intrinsic hand muscles
Weakness of the intrinsic hand muscles 		0.100 Biomarker phenotype HPO
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs 		0.100 Biomarker phenotype HPO
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting 		0.100 Biomarker phenotype HPO
CUI: C1836156
Disease: Progressive proximal muscle weakness
Progressive proximal muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C1836609
Disease: Progressive distal muscle weakness
Progressive distal muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C1837323
Disease: Decreased Achilles reflex
Decreased Achilles reflex 		0.100 Biomarker phenotype HPO
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C1864716
Disease: Intrinsic hand muscle atrophy
Intrinsic hand muscle atrophy 		0.100 Biomarker phenotype HPO
CUI: C1866012
Disease: Proximal muscle weakness in upper limbs
Proximal muscle weakness in upper limbs 		0.100 Biomarker phenotype HPO
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		0.100 Biomarker phenotype HPO
CUI: C2228039
Disease: Ankle weakness
Ankle weakness 		0.100 Biomarker phenotype HPO
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex 		0.100 Biomarker phenotype HPO
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		0.100 Biomarker phenotype HPO