Hyperglycinemia, Nonketotic
An autosomal recessive metabolic disorder caused by deficiencies in the mitochondrial GLYCINE cleavage system.
Year introduced: 2000
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Subheadings:
Tree Number(s): C10.228.140.163.100.375, C16.320.565.100.477, C16.320.565.189.375, C18.452.132.100.375, C18.452.648.100.477, C18.452.648.189.375
MeSH Unique ID: D020158
Entry Terms:
- Hyperglycinemias, Nonketotic
- Nonketotic Hyperglycinemias
- Non-ketotic Hyperglycinemia
- Hyperglycinemia, Non-ketotic
- Hyperglycinemias, Non-ketotic
- Non ketotic Hyperglycinemia
- Non-ketotic Hyperglycinemias
- Nonketotic Hyperglycinemia
- Glycine Encephalopathy
- Encephalopathies, Glycine
- Encephalopathy, Glycine
- Glycine Encephalopathies
- Hyperglycinemia, Nonketotic, Type I
- Nonketotic Hyperglycinemia, Type I
- Type I Nonketotic Hyperglycinemia
- Hyperglycinemia, Nonketotic, Type II
- Nonketotic Hyperglycinemia, Type II
- Type II Nonketotic Hyperglycinemia
- Hyperglycinemia, Nonketotic, Type III
- Nonketotic Hyperglycinemia, Type III
- Type III Nonketotic Hyperglycinemia
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