E72.4 – Disorders of ornithine metabolism
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Type 1 Excludes
hereditary choroidal dystrophy (H31.2-)
Applicable To
Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome
Ornithinemia (types I, II)
Ornithine transcarbamylase deficiency
GEM Conversion to ICD-9 CM
Fs: 10000
–
Disorders of urea cycle metabolism
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Deficiency, deficient
Disorder
(of)
See also Disease
Disturbance
(s)
See also Disease
Hyperaminoaciduria
Ornithinemia
(Type I) (Type II)
E72.4
Syndrome
See also Disease
Sibling Codes
Parent Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| E00-E89 | Endocrine, nutritional and metabolic diseases (E00-E89) |
| E70-E88 | Metabolic disorders (E70-E88) |
| E72 | Other disorders of amino-acid metabolism |
| 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
|