Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Hereditary Motor and Sensory-Neuropathy Type II
disease 0.100 None 1.000 154 87 1990 2018
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
disease 0.100 None 1.000 16 2 1990 2013
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Cardiomyopathy, Hypertrophic, Familial
disease 0.100 None 1.000 3 2 2006 2014
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0005890
Disease: Body Height
Body Height
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0349782
Disease: Ischemic cardiomyopathy
Ischemic cardiomyopathy
disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Second degree atrioventricular block
disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder)
disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1184923
Disease: Lumbar hyperlordosis
Lumbar hyperlordosis
disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature
disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
phenotype 0.100 None 1.000 1 1 2019 2019
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1837758
Disease: Bird-like facies
Bird-like facies
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Progressive clavicular acroosteolysis
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Loss of subcutaneous adipose tissue in limbs
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1837770
Disease: Sparse hair
Sparse hair
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1837463
Disease: Narrow face
Narrow face
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
disease 0.100 None 0 2
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1833762
Disease: Decreased calvarial ossification
Decreased calvarial ossification
phenotype 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia
disease 0.100 None 0 0
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1834481
Disease: CARDIOMYOPATHY, DILATED, 1S
CARDIOMYOPATHY, DILATED, 1S
disease 0.100 None 0 3
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
lamin A/C 0.384 0.885 1.00
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs
phenotype 0.100 None 0 0