LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CARDIOMYOPATHY, DILATED, 1C (disorder)
disease Cardiovascular Diseases Disease or Syndrome 3 4 0.900 None 1.000 2 4 2003 2004
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 925 294 0.410 None 1.000 1 2017 2017
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 61 24 0.410 None 1.000 1 2 2013 2013
CUI: C4721886
Disease: MYOPATHY, MYOFIBRILLAR, 4
MYOPATHY, MYOFIBRILLAR, 4
disease Disease or Syndrome 1 2 0.400 None 1.000 1 2 2005 2005
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group Cardiovascular Diseases Disease or Syndrome 512 509 0.330 None 1.000 3 2004 2009
Myopathy, Myofibrillar, Zasp-Related
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 1 0.310 None 1.000 2 2011 2017
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction
disease Cardiovascular Diseases Disease or Syndrome 35 26 0.310 None 1.000 1 1 2012 2012
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 83 47 0.300 None 1.000 2 2003 2004
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 6 5 0.300 None 1.000 1 2015 2015
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 20 48 0.200 None 1.000 1 2001 2001
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 280 67 0.200 None 1.000 1 2001 2001
CUI: C0027127
Disease: Myotonia Congenita
Myotonia Congenita
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 9 38 0.200 None 1.000 1 2001 2001
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24
disease Disease or Syndrome 1 0.200 None 0
CUI: C3152137
Disease: LEFT VENTRICULAR NONCOMPACTION 3
LEFT VENTRICULAR NONCOMPACTION 3
disease Disease or Syndrome 1 0.200 None 0
CUI: C0026848
Disease: Myopathy
Myopathy
group Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 634 166 0.110 None 1.000 1 2006 2006
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases
group Nervous System Diseases Disease or Syndrome 171 50 0.100 None 1.000 8 1 2005 2017
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
phenotype Organ or Tissue Function 272 1169 0.100 None 1.000 1 1 2015 2015
Weakness of long finger extensor muscles
phenotype Finding 18 0.100 None 0
CUI: C1837323
Disease: Decreased Achilles reflex
Decreased Achilles reflex
phenotype Finding 7 0.100 None 0
CUI: C1836609
Disease: Progressive distal muscle weakness
Progressive distal muscle weakness
phenotype Finding 14 4 0.100 None 0
Progressive proximal muscle weakness
phenotype Finding 28 3 0.100 None 0
CUI: C1836057
Disease: Muscle fiber splitting
Muscle fiber splitting
phenotype Finding 13 0.100 None 0
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs
phenotype Finding 19 1 0.100 None 0
Weakness of the intrinsic hand muscles
phenotype Finding 21 0.100 None 0
Fatigable weakness of distal limb muscles
phenotype Finding 8 0.100 None 0