ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2E — Syndromes with structural anomalies due to inborn errors of...
ICD-11 LD2E — Syndromes with structural anomalies due to inborn errors of metabolism
The diagnosis has no description.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code LD2E contains 7 clarifying diagnoses:
- 5C52.10 — Disorders of cholesterol synthesis
- 5C53.02 — Pyruvate dehydrogenase complex deficiency
- 5C54 — Inborn errors of glycosylation or other specified protein modification
It contains 5 clarifying diagnoses. - 5C56.01 — Fabry disease
- 5C56.20 — Mucolipidosis
- 5C56.21 — Oligosaccharidosis
- 5C56.3 — Mucopolysaccharidosis
It contains 6 clarifying diagnoses.
The diagnosis is included in 15 other classes.
- 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)