E72.23
BillableCitrullinemia
Citrullinemia
Coding Notes
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.-)
- disorders of ornithine metabolism (E72.4)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Citrullinaemia, subacute type3140001
- Citrullinemia, subacute type3140001
- Citrullinaemia, neonatal type30529005
- Citrullinemia, neonatal type30529005
- Argininosuccinate synthase deficiency124711003
- Deficiency of argininosuccinate synthase124711003
- Deficiency of citrulline-aspartate ligase124711003
- Citrullinuria398630005
- Citrullinaemia398680004
- Citrullinemia398680004
- Citrin deficiency429735007
- SLC25A13 related citrin deficiency429735007
- Solute carrier family 25 member 13 related citrin deficiency429735007
- Adult onset citrin deficiency716863007
- Adult onset type 2 citrullinaemia716863007
- Adult onset type 2 citrullinemia716863007
- Citrullinaemia type II716863007
- Citrullinemia type II716863007
- ASS1-gene related citrullinaemia type I1149103000
- ASS1-gene related citrullinemia type I1149103000
- Argininosuccinate synthase 1-gene related citrullinaemia type I1149103000
- Argininosuccinate synthase 1-gene related citrullinemia type I1149103000
- Citrullinaemia type 11149103000
- Citrullinaemia type I1149103000
- Citrullinemia type 11149103000
- Citrullinemia type I1149103000
- Classic citrullinaemia1149103000
- Classic citrullinemia1149103000
- Late-onset citrullinaemia type 11264112006
- Late-onset citrullinaemia type I1264112006
- Late-onset citrullinemia type 11264112006
- Late-onset citrullinemia type I1264112006
- Neonatal metabolic acidaemia16068331000119102
- Neonatal metabolic acidemia16068331000119102
UMLS
- ARGININOSUCCINATE SYNTHASE DEFIC DISC0175683
- ARGININOSUCCINATE SYNTHETASE DEFICIENCYC0175683
- ARGININOSUCCINIC ACID SYNTHASE DEFIC DISC0175683
- ARGININOSUCCINIC ACID SYNTHETASE DEFIC DISC0175683
- ASS DEFICIENCYC0175683
- ASS DeficienciesC0175683
- ASS DeficiencyC0175683
- ASS deficiencyC0175683
- Argininosuccinate Synthase Deficiency DiseaseC0175683
- Argininosuccinate Synthetase DeficienciesC0175683
- Argininosuccinate Synthetase DeficiencyC0175683
- Argininosuccinate synthase deficiencyC0175683
- Argininosuccinate synthetase deficiencyC0175683
- Argininosuccinic Acid Synthase Deficiency DiseaseC0175683
- Argininosuccinic Acid Synthetase DeficiencyC0175683
- Argininosuccinic Acid Synthetase Deficiency DiseaseC0175683
- CITC0175683
- CITRULLINURIAC0175683
- CitrullinaemiaC0175683
- CitrullinemiaC0175683
- Citrullinemia (disorder)C0175683
- CitrullinemiasC0175683
- CitrullinuriaC0175683
- CitrullinuriasC0175683
- DEFIC DIS ARGININOSUCCINATE SYNTHASEC0175683
- DEFIC DIS ARGININOSUCCINIC ACID SYNTHASEC0175683
- Deficiencies, Argininosuccinate SynthetaseC0175683
- Deficiency Disease, Argininosuccinate SynthaseC0175683
- Deficiency Disease, Argininosuccinic Acid SynthaseC0175683
- Deficiency of argininosuccinate synthaseC0175683
- Deficiency of argininosuccinate synthase (disorder)C0175683
- Deficiency of citrulline-aspartate ligaseC0175683
- Deficiency, ASSC0175683
- Deficiency, Argininosuccinate SynthetaseC0175683
- arginosuccinate synthetase deficiencyC0175683
- ass deficiencyC0175683
- citrullinaemiaC0175683
- citrullinemiaC0175683
Frequently Asked Questions
What is the ICD-10 code for citrullinemia?
The ICD-10-CM code for citrullinemia is E72.23. The full clinical description is "Citrullinemia". E72.23 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.23 mean?
ICD-10-CM code E72.23 represents "Citrullinemia". 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 E72.23 a billable code?
Yes, E72.23 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.23 in?
E72.23 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.23?
E72.23 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 E72.23 map to?
E72.23 maps to 10 SNOMED CT concepts: 1149103000, 716863007, 124711003, 429735007, 398680004, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.23?
E72.23 is linked to 1 UMLS Concept Unique Identifier: C0175683. 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.