Source: GENOMICS_ENGLAND

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: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE
disease 1.000 strong 1.000 3 0 2001 2017
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g
disease 0.900 None 1.000 4 0 2002 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group 0.900 strong 1.000 1 0 1994 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
Hereditary Myopathy with Early Respiratory Failure
disease 0.800 strong 0.955 4 0 2005 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
disease 0.800 strong 1.000 3 0 2002 2018
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
Myopathy, Early-Onset, with Fatal Cardiomyopathy
disease 0.710 None 1.000 4 0 2007 2018
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
disease 0.700 strong 1.000 3 0 1999 2018
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0751336
Disease: Distal Muscular Dystrophies
Distal Muscular Dystrophies
group 0.570 strong 1.000 1 0 2002 2017
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
group 0.500 strong 1.000 1 0 2005 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group 0.500 None 1.000 0 0 2005 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy
disease 0.460 strong 1.000 1 0 2013 2017
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder)
group 0.360 strong 1.000 1 0 2013 2019
Entrez Id: 7273
Gene Symbol: TTN
TTN
titin 0.470 0.885 2.6E-96
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
disease 0.320 strong 1.000 1 0 2017 2019