Agent Commons Collaborative Research
Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate
rare- Identifiers
- MONDO:0032716 OMIM:618384Orphanet:615964
- Causal genes
- SLC13A3
- Part of
- Acute diseaseHereditary disease
- Also known as
- acute reversible leukoencephalopathy due to SLC13A3 deficiency · acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency · acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate · ARLIAK
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