Pelizaeus-Merzbacher-like due to GJC2 mutation (Q93664): Difference between revisions
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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 GJC2 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1983099839 |
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| English | Pelizaeus-Merzbacher-like due to GJC2 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 GJC2 gene. |
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CID11:ID_1983099839
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dki-india-ID_1983099839
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