E72.4
BillableDisorders of ornithine metabolism
Disorders of ornithine metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome
- Ornithinemia (types I, II)
- Ornithine transcarbamylase deficiency
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- disorders of:
- aromatic amino-acid metabolism (E70.-)
- branched-chain amino-acid metabolism (E71.0-E71.2)
- fatty-acid metabolism (E71.3)
- purine and pyrimidine metabolism (E79.-)
- gout (M1A.-, M10.-)
- hereditary choroidal dystrophy (H31.2-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hyperammonaemia9360008
- Hyperammonemia9360008
- HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome30287008
- HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome30287008
- Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome30287008
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome30287008
- SLC25A15-gene related hyperornithinaemia, hyperammonaemia, homocitrullinuria syndrome30287008
- SLC25A15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndrome30287008
- Solute carrier family 25 member 15-gene related hyperornithinaemia, hyperammonaemia, homocitrullinuria syndrome30287008
- Solute carrier family 25 member 15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndrome30287008
- Hyperornithinaemia33985005
- Hyperornithinemia33985005
- Deficiency of citrulline phosphorylase80908008
- Deficiency of ornithine carbamoyltransferase80908008
- Deficiency of ornithine transcarbamylase80908008
- OCT (ornithine carbamoyltransferase) deficiency80908008
- OTC (ornithine transcarbamylase) deficiency80908008
- OTC-gene related ornithine carbamoyltransferase deficiency80908008
- Ornithine carbamoyltransferase deficiency80908008
- Ornithine transcarbamoylase deficiency80908008
- Ornithine transcarbamylase deficiency80908008
- Disorder of ornithine metabolism237928008
- Ornithine metabolism disorder237928008
- Deficiency of ornithine-oxo-acid aminotransferase276426004
- OAT - Ornithine oxo-acid aminotransferase deficiency276426004
- OAT deficiency276426004
- OKT deficiency276426004
- Ornithine aminotransferase deficiency276426004
- Ornithine ketoacid transaminase deficiency276426004
- Ornithine oxo-acid aminotransferase deficiency276426004
- Ornithine-delta-aminotransferase deficiency276426004
- Ornithine-oxo-acid amino acid transferase deficiency276426004
UMLS
- HHH syndromeC0268540
- HHHC0268540
- HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndromeC0268540
- HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeC0268540
- HHH SYNDROMEC0268540
- HHHSC0268540
- HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROMEC0268540
- Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndromeC0268540
- Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndromeC0268540
- Hyperornithinemia-Hyperammonemia-Homocitrullinemia SyndromeC0268540
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria SyndromeC0268540
- Hyperornithinemia-hyperammonemia-homocitrullinuriaC0268540
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeC0268540
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder)C0268540
- ORNITHINE TRANSLOCASE DEFICIENCYC0268540
- Ornithine translocase deficiencyC0268540
- SLC25A15-gene related hyperornithinaemia, hyperammonaemia, homocitrullinuria syndromeC0268540
- SLC25A15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndromeC0268540
- Solute carrier family 25 member 15-gene related hyperornithinaemia, hyperammonaemia, homocitrullinuria syndromeC0268540
- Solute carrier family 25 member 15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndromeC0268540
- Triple H SyndromeC0268540
- Triple H syndromeC0268540
- DEFIC DIS ORNITHINE CARBAMOYLTRANSFERASEC0268542
- DEFIC DIS ORNITHINE TRANSCARBAMYLASEC0268542
- Deficiencies, OTCC0268542
- Deficiencies, Ornithine TranscarbamylaseC0268542
- Deficiency Disease, Ornithine CarbamoyltransferaseC0268542
- Deficiency Disease, Ornithine TranscarbamylaseC0268542
- Deficiency of citrulline phosphorylaseC0268542
- Deficiency of ornithine carbamoyltransferaseC0268542
- Deficiency of ornithine transcarbamylaseC0268542
- Deficiency, OTCC0268542
- Deficiency, Ornithine TranscarbamylaseC0268542
- OCT (ornithine carbamoyltransferase) deficiencyC0268542
- ORNITHINE CARBAMOYLTRANSFERASE DEFIC DISC0268542
- ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCYC0268542
- ORNITHINE TRANSCARBAMYLASE DEFIC DISC0268542
- ORNITHINE TRANSCARBAMYLASE DEFICIENCYC0268542
- ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TOC0268542
- OTC (ornithine transcarbamylase) deficiencyC0268542
- OTC DEFICIENCYC0268542
- OTC DeficienciesC0268542
- OTC DeficiencyC0268542
- OTC-gene related ornithine carbamoyltransferase deficiencyC0268542
- Ornithine Carbamoyltransferase DeficiencyC0268542
- Ornithine Carbamoyltransferase Deficiency DiseaseC0268542
- Ornithine Transcarbamylase DeficienciesC0268542
- Ornithine Transcarbamylase DeficiencyC0268542
- Ornithine Transcarbamylase Deficiency DiseaseC0268542
- Ornithine Transcarbamylase Deficiency, Hyperammonemia Due ToC0268542
- Ornithine carbamoyltransferase deficiencyC0268542
- Ornithine carbamoyltransferase deficiency (disorder)C0268542
- Ornithine transcarbamoylase deficiencyC0268542
- Ornithine transcarbamylase deficiencyC0268542
- congenital hyperammonemia type IIC0268542
- octdC0268542
- ornithine carbamoyltransferase deficiencyC0268542
- ornithine carbamoyltransferase deficiency (OCTD)C0268542
- ornithine transcarbamylase deficiencyC0268542
- Disorder of ornithine metabolismC0342690
- Disorder of ornithine metabolism (disorder)C0342690
- Disorders of ornithine metabolismC0342690
- Ornithine metabolism disorderC0342690
- Ornithinemia (types I, II)C2874262
Frequently Asked Questions
What is the ICD-10 code for disorders of ornithine metabolism?
The ICD-10-CM code for disorders of ornithine metabolism is E72.4. The full clinical description is "Disorders of ornithine metabolism". E72.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.4 mean?
ICD-10-CM code E72.4 represents "Disorders of ornithine metabolism". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E72.4 a billable code?
Yes, E72.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.4 in?
E72.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.4?
E72.4 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 10 more.
What SNOMED CT codes does E72.4 map to?
E72.4 maps to 6 SNOMED CT concepts: 80908008, 276426004, 237928008, 30287008, 9360008, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.4?
E72.4 is linked to 4 UMLS Concept Unique Identifiers: C0268540, C0268542, C0342690, C2874262. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.