Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
TNNT3
(HGNC:11950)
Sheldon-hall syndrome
(MONDO_0011128)
 Moderate
CD70
(HGNC:11937)
severe combined immunodeficiency due to CD70 deficiency
(MONDO_0034054)
 Limited
TNNT2
(HGNC:11949)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Definitive
TNNT2
(HGNC:11949)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
TNNT2
(HGNC:11949)
dilated cardiomyopathy
(MONDO_0005021)
 Definitive
TNNT2
(HGNC:11949)
cardiomyopathy
(MONDO_0004994)
 Strong
TNNT1
(HGNC:11948)
nemaline myopathy 5
(MONDO_0011539)
 Strong
TNNI3
(HGNC:11947)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
TNNI3
(HGNC:11947)
dilated cardiomyopathy 2A
(MONDO_0012746)
 Limited
TNNI3
(HGNC:11947)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
TNNI2
(HGNC:11946)
Sheldon-hall syndrome
(MONDO_0011128)
 Strong
TNNC1
(HGNC:11943)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Limited
TNNC1
(HGNC:11943)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Moderate
TNNC1
(HGNC:11943)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
FASLG
(HGNC:11936)
autoimmune lymphoproliferative syndrome type 1
(MONDO_0011158)
 Moderate
TNFSF13
(HGNC:11928)
common variable immunodeficiency
(MONDO_0015517)
 Limited
TNFSF4
(HGNC:11934)
systemic lupus erythematosus
(MONDO_0007915)
 Strong
TNFSF12
(HGNC:11927)
common variable immunodeficiency
(MONDO_0015517)
 Limited
CD27
(HGNC:11922)
lymphoproliferative syndrome 2
(MONDO_0014054)
 Moderate
TNFSF11
(HGNC:11926)
autosomal recessive osteopetrosis
(MONDO_0019026)
 Strong
Showing 3801–3820 of 6699