| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 2q31.2 | Cardiomyopathy, dilated, 1G | 604145 | AD | 3 |
| Cardiomyopathy, familial hypertrophic, 9 | 613765 | AD | 3 | |
| Congenital myopathy 5 with cardiomyopathy | 611705 | AR | 3 | |
| Muscular dystrophy, limb-girdle, autosomal recessive 10 | 608807 | AR | 3 | |
| Myopathy, myofibrillar, 9, with early respiratory failure | 603689 | AD | 3 | |
| Tibial muscular dystrophy, tardive | 600334 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 2q31.2 | Myopathy, myofibrillar, 9, with early respiratory failure | 603689 | AD | 3 | TTN | 188840 |
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