Orphanet: Leigh syndrome with leukodystrophy

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Leigh syndrome with leukodystrophy

ORPHA:255241

Classification level: Disorder

Synonym(s):
- Infantile subacute necrotizing encephalopathy with leukodystrophy
- Leigh disease with leukodystrophy
Prevalence: -
Inheritance: Autosomal recessive
Age of onset: Infancy, Neonatal
ICD-10: G31.8
OMIM: 252010 256000 616277 618222 618224 618225 618226 618228 618229 618230 618233 618235 618239 618240 618241 618243 618244 618248 618249 618257
UMLS: -
MeSH: -
GARD: -
MedDRA: -

Summary

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Leigh syndrome with leukodystrophy

ORPHA:255241

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