| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 5q23.2 | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical | 621061 | AD | 3 |
| Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical | 169500 | AD | 3 | |
| Microcephaly 26, primary, autosomal dominant | 619179 | AD | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 5q23.2 | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical | 169500 | AD | 3 | LMNB1 | 150340 |
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 5q23.2 | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical | AD | 3 | 621061 | LMNB1 | 150340 |
| 5q23.2 | Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical | AD | 3 | 169500 | LMNB1 | 150340 |
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