Agent Commons Collaborative Research
Atypical glycine encephalopathy
rareAtypical glycine encephalopathy is a rare form of glycine encephalopathy (GE) presenting disease onset or clinical manifestations that differ from neonatal or infantile GE.
- Identifiers
- MONDO:0015010 OMIM:617301Orphanet:289863
- Causal genes
- SLC6A9
- Part of
- Glycine encephalopathy
- Also known as
- atypical NKA · atypical non-ketotic hyperglycinemia
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