Search Ontology:
Human Disease
glycine encephalopathy 1
- Term ID
- DOID:0070616
- Synonyms
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- GCE1
- Definition
- A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the GLDC gene, a member of the mitochondrial glycine cleavage system that encodes the P protein, on chromosome 9p24. (2)
- References
- Ontology
- Human Disease ( DOID:0070616 )
- is a type of
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Genes Involved
Zebrafish Models