E72.4
Disorders of ornithine metabolism
- Type 1 Excludes:
- Hereditary Choroidal Dystrophy (H31.2-)
Applicable To:
- Hyperammonemia-Hyperornithinemia-Homocitrullinemia Syndrome
- Ornithinemia (types I, II)
- Ornithine Transcarbamylase Deficiency
The following code(s) above E72.4 may contain annotation back-references that may be applicable to E72.4:
- Endocrine, nutritional and metabolic diseases (E00-E89)
Diagnosis Index