| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 19q13.2 | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | 617519 | AR | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 19q13.2 | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | 617519 | AR | 3 | SPTBN4 | 606214 |
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