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Gene–disease association summaries
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
|
|