All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02481 CMD1G cardiomyopathy, dilated, type 1G (CMD-1G) 604145 - 2 1 TTN - -
03425 CMH9 cardiomyopathy, hypertrophic, familial, type 9 (CMH-9) 613765 AD - - TTN - -
03046 CMYO5;SALMY myopathy, congenital, type 5, with cardiomyopathy 611705 AR 9 9 TTN - -
02795 LGMDR10;LGMD2J dystrophy, muscular, limb-girdle, autosomal recessive, type 10 (LGMD2J) 608807 AR 32 31 TTN - -
02465 MFM9 myopathy, myofibrillar, 9, with early respiratory failure 603689 AD 29 27 TTN - -
03741 PMGYS Polymicrogyria with seizures (PMGYS) 614833 AR 3 3 RTTN - -
00101 TMD dystrophy, muscular, tibial (TMD) 600334 AD 11 12 TTN - -
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