TTN-AS1, TTN antisense RNA 1, 100506866

N. diseases: 78; N. variants: 567
Source: CLINVAR ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		0.100 CausalMutation phenotype CLINVAR
CUI: C0013404
Disease: Dyspnea
Dyspnea 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0013404
Disease: Dyspnea
Dyspnea 		0.100 CausalMutation phenotype CLINVAR
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.100 GeneticVariation disease CLINVAR
CUI: C0018808
Disease: Heart murmur
Heart murmur 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 GeneticVariation group CLINVAR
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure 		0.100 CausalMutation disease CLINVAR
CUI: C0023212
Disease: Left-Sided Heart Failure
Left-Sided Heart Failure 		0.100 GeneticVariation disease CLINVAR
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation phenotype CLINVAR
CUI: C0026848
Disease: Myopathy
Myopathy 		0.100 CausalMutation group CLINVAR
CUI: C0026848
Disease: Myopathy
Myopathy 		0.100 GeneticVariation group CLINVAR
CUI: C0026850
Disease: Muscular Dystrophy
Muscular Dystrophy 		0.100 GeneticVariation disease CLINVAR
CUI: C0027092
Disease: Myopia
Myopia 		0.100 GeneticVariation disease CLINVAR
CUI: C0027092
Disease: Myopia
Myopia 		0.100 CausalMutation disease CLINVAR
CUI: C0030252
Disease: Palpitations
Palpitations 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 GeneticVariation disease CLINVAR
CUI: C0039070
Disease: Syncope
Syncope 		0.100 CausalMutation phenotype CLINVAR
CUI: C0039070
Disease: Syncope
Syncope 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		0.100 GeneticVariation disease CLINVAR
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		0.100 CausalMutation disease CLINVAR
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		0.100 GeneticVariation disease CLINVAR
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		0.100 GeneticVariation disease CLINVAR
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.100 GeneticVariation disease CLINVAR