| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 1q22 | Cardiomyopathy, dilated, 1A | 115200 | AD | 3 |
| Charcot-Marie-Tooth disease, type 2B1 | 605588 | AR | 3 | |
| Emery-Dreifuss muscular dystrophy 2, autosomal dominant | 181350 | AD | 3 | |
| Emery-Dreifuss muscular dystrophy 3, autosomal recessive | 616516 | AR | 3 | |
| Heart-hand syndrome, Slovenian type | 610140 | AD | 3 | |
| Hutchinson-Gilford progeria | 176670 | AD | 3 | |
| Lipodystrophy, familial partial, type 2 | 151660 | AD | 3 | |
| Malouf syndrome | 212112 | AD | 3 | |
| Mandibuloacral dysplasia | 248370 | AR | 3 | |
| Muscular dystrophy, congenital | 613205 | AD | 3 | |
| Restrictive dermopathy 2 | 619793 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 1q22 | Cardiomyopathy, dilated, 1A | 115200 | AD | 3 | LMNA | 150330 |
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