| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 2q24.3 | Erythermalgia, primary | 133020 | AD | 3 |
| Insensitivity to pain, congenital | 243000 | AR | 3 | |
| Neuropathy, hereditary sensory and autonomic, type IID | 243000 | AR | 3 | |
| Paroxysmal extreme pain disorder | 167400 | AD | 3 | |
| Small fiber neuropathy | 133020 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 2q24.3 | Paroxysmal extreme pain disorder | 167400 | AD | 3 | SCN9A | 603415 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 2q24.3 | Small fiber neuropathy | 133020 | AD | 3 | SCN9A | 603415 |
| 2q24.3 | Erythermalgia, primary | 133020 | AD | 3 | SCN9A | 603415 |
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