| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 17p12 | ?Neuropathy, inflammatory demyelinating | 139393 | ?AD | 3 |
| Charcot-Marie-Tooth disease, type 1A | 118220 | AD | 3 | |
| Charcot-Marie-Tooth disease, type 1E | 118300 | AD | 3 | |
| Dejerine-Sottas disease | 145900 | AD, AR | 3 | |
| Neuropathy, recurrent, with pressure palsies | 162500 | AD | 3 | |
| Roussy-Levy syndrome | 180800 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 17p12 | Neuropathy, recurrent, with pressure palsies | 162500 | AD | 3 | PMP22 | 601097 |
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