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D-glyceric aciduria
Summary
- Synonym
-
- D-glycerate kinase deficiency
- D-glyceric acidemia
- D-glycericacidemia
- deficiency of glycerate kinase
- non ketotic hyperglycinemia syndrome
- Definition
- An inherited metabolic disorder characterized by impaired serine and fructose metabolism resulting in elevated excretion of D-glyceric acid that has_material_basis_in homozygous or compound heterozygous mutation in the GLYCTK gene on chromosome 3p21.2.
- Super Class
- autosomal recessive disease inherited metabolic disorder
External Links
- Disease Ontology
- DOID:0111626
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- OMIM
- GARD
- WikiPathways (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003108 | Hyperglycinuria |
| HP:0001257 | Spasticity |
| HP:0100704 | Cerebral visual impairment |
| HP:0000729 | Autistic behavior |
| HP:0011344 | Severe global developmental delay |
| HP:0002072 | Chorea |
| HP:0000253 | Progressive microcephaly |
| HP:0008288 | Nonketotic hyperglycinemia |
| HP:0001336 | Myoclonus |
| HP:0012444 | Brain atrophy |
