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Leigh syndrome with leukodystrophy
ORPHA:255241
- Synonym(s):
- Infantile subacute necrotizing encephalopathy with leukodystrophy
- Leigh disease with leukodystrophy
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: G31.8
- ICD-11: 5C53.24
- OMIM: 252010 256000 616277 618222 618224 618225 618226 618228 618229 618230 618233 618235 618239 618240 618241 618243 618244 618248 618249
- UMLS: C5679635
- MeSH: -
- GARD: -
- MedDRA: -
Summary
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Leigh syndrome
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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