All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03046 - myopathy, early-onset, with fatal cardiomyopathy 611705 9 9 TTN - -
02481 CMD-1G cardiomyopathy, dilated, type 1G (CMD-1G) 604145 0 0 TTN - -
03425 CMH-9 cardiomyopathy, hypertrophic, familial, type 9 (CMH-9) 613765 0 0 TTN - -
02465 HMERF myopathy, hereditary with early respiratory failure (HMERF) 603689 27 27 TTN - -
02795 LGMD-2J dystrophy, muscular, limb-girdle, type 2J (LGMD-2J) 608807 19 19 TTN - -
03741 PMGYS Polymicrogyria with seizures (PMGYS) 614833 1 1 RTTN - -
00101 TMD dystrophy, muscular, tibial (TMD) 600334 11 11 TTN - -