LD2E Syndromes with structural anomalies due to inborn errors of metabolism
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- Disorders of cholesterol synthesis (5C52.10)
- Pyruvate dehydrogenase complex deficiency (5C53.02)
- Inborn errors of glycosylation or other specified protein modification (5C54)
- Fabry disease (5C56.01)
- Mucolipidosis (5C56.20)
- Oligosaccharidosis (5C56.21)
- Mucopolysaccharidosis (5C56.3)
- Pseudo-Zellweger syndrome (5C57.Y)
- Hypophosphatasia (5C64.3)
- Classical homocystinuria (5C50.B)
- Encephalopathy due to sulfite oxidase deficiency (5C50.B)
- Mucosulfatidosis (5C56.0Y)
- Zellweger syndrome (5C57.0)
- Infantile Refsum disease (5C57.1)
- Menkes disease (5C64.0Y)
synonyms
- Syndromes with structural anomalies due to inborn errors of metabolism
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