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Stats

Total associations
6681
Unique genes
4239
Unique diseases
3297
Gene–disease association summaries
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Gene Disease Score Actions
MYH6
(HGNC:7576)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Moderate
MYH7
(HGNC:7577)
dilated cardiomyopathy
(MONDO_0005021)
 Strong
MYH6
(HGNC:7576)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
MYH3
(HGNC:7573)
contractures, pterygia, and variable skeletal fusions syndrome 1B
(MONDO_0020746)
 Strong
MYH3
(HGNC:7573)
Sheldon-hall syndrome
(MONDO_0011128)
 Strong
MYH3
(HGNC:7573)
spondylocarpotarsal synostosis syndrome
(MONDO_0010094)
 Strong
MYH3
(HGNC:7573)
Freeman-Sheldon syndrome
(MONDO_0008675)
 Definitive
MVK
(HGNC:7530)
disseminated superficial actinic porokeratosis
(MONDO_0019212)
 Strong
MYCN
(HGNC:7559)
Feingold syndrome type 1
(MONDO_0008115)
 Definitive
MYD88
(HGNC:7562)
pyogenic bacterial infections due to MyD88 deficiency
(MONDO_0012839)
 Moderate
MYH3
(HGNC:7573)
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
(MONDO_0008338)
 Moderate
MYBPC3
(HGNC:7551)
arrhythmogenic right ventricular cardiomyopathy
(MONDO_0016587)
 Disputed
MYBPC3
(HGNC:7551)
hypertrophic cardiomyopathy
(MONDO_0005045)
 Definitive
MYBPC3
(HGNC:7551)
dilated cardiomyopathy
(MONDO_0005021)
 Moderate
MYBPC3
(HGNC:7551)
atrial fibrillation
(MONDO_0004981)
 Limited
MVK
(HGNC:7530)
mevalonic aciduria
(MONDO_0012481)
 Definitive
MVK
(HGNC:7530)
hyperimmunoglobulinemia D with periodic fever
(MONDO_0009849)
 Definitive
TRIM37
(HGNC:7523)
mulibrey nanism
(MONDO_0009664)
 Definitive
MVD
(HGNC:7529)
disseminated superficial actinic porokeratosis
(MONDO_0019212)
 Moderate
MUTYH
(HGNC:7527)
hereditary breast carcinoma
(MONDO_0016419)
 Disputed
Showing 701–720 of 6681