Overview
Leucodystrophy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Galactosylceramide beta-galactosidase deficiency(child)
Neuroaxonal leukodystrophy(child)
Phytanic acid storage disease(child)
Adult onset autosomal dominant leucodystrophy(child)
RNA polymerase III-related leukodystrophy(child)
Progressive encephalopathy with severe infantile anorexia(child)
Pelizaeus Merzbacher like disease(child)
X-linked spastic paraplegia type 2(child)
Dermatoleukodystrophy(child)
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease(child)
TUBB4A-related leukodystrophy(child)
HBSL - hypomyelination, brain stem, spinal cord, leg spasticity(child)
Muscle eye brain disease with bilateral multicystic leucodystrophy(child)
Pelizaeus-Merzbacher disease(child)
Alexander's disease(child)
Vanishing white matter disease(child)
C11ORF73-related autosomal recessive hypomyelinating leukodystrophy(child)
VPS11-related autosomal recessive hypomyelinating leukodystrophy(child)
Multiple mitochondrial dysfunctions syndrome type 4(child)
4H leucodystrophy(child)
Quick Facts
- SNOMED CT
- 192781003
- UMLS CUI
- C0023520
- Fully Specified Name
- Leukodystrophy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.