TNNI3, troponin I3, cardiac type, 7137

N. diseases: 9; N. variants: 39
Source: CLINVAR ×
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.
CUI: C1860752
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 		disease Disease or Syndrome 1 12 0.900 strong 1.000 11 12 1997 2019
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		disease Cardiovascular Diseases Disease or Syndrome 2 10 0.800 strong 1.000 5 9 2003 2019
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 29 468 0.700 definitive 0.991 76 19 1988 2019
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 6 15 0.700 None 1.000 15 5 2003 2017
CUI: C2678474
Disease: CARDIOMYOPATHY, DILATED, 2A (disorder)
CARDIOMYOPATHY, DILATED, 2A (disorder) 		disease Cardiovascular Diseases Disease or Syndrome 1 2 0.700 strong 1.000 5 2 2003 2019
CUI: C2750091
Disease: Cardiomyopathy, Dilated, 1FF
Cardiomyopathy, Dilated, 1FF 		disease Cardiovascular Diseases Disease or Syndrome 1 5 0.700 strong 1.000 5 5 2003 2019
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		group Cardiovascular Diseases Disease or Syndrome 45 172 0.690 None 1.000 0 5 2006 2018
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 24 332 0.500 None 1.000 59 18 1997 2017
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group Cardiovascular Diseases Disease or Syndrome 43 443 0.430 None 1.000 3 3 2003 2017