Pelizaeus-Merzbacher-like due to SLC16A2 mutation (Q93659): Difference between revisions
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Latest revision as of 08:45, 16 August 2026
Pelizaeus-Merzbacher like disease (PMLD) is an autosomal recessive leukodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease (PMD; ). This type is due to a mutation in the SLC16A2 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1381085790 |
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| English | Pelizaeus-Merzbacher-like due to SLC16A2 mutation |
Pelizaeus-Merzbacher like disease (PMLD) is an autosomal recessive leukodystrophy sharing identical clinical and radiological features as X-linked Pelizaeus-Merzbacher disease (PMD; ). This type is due to a mutation in the SLC16A2 gene. |
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CID11:ID_1381085790
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dki-india-ID_1381085790
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Concluído
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15 August 2026
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