E72.23

Billable

Citrullinemia

Citrullinemia

Status

Billable / Specific

Block

E70-E88

Parent Code

E72.2

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
E72.20

Disorder of urea cycle metabolism, unspecified

BillableE72.21

Argininemia

BillableE72.22

Arginosuccinic aciduria

BillableE72.29

Other disorders of urea cycle metabolism

Billable
Also Known As / Clinical Terms(129)

SNOMED CT

UMLS

Clinical Terms

  • Classic citrullinaemia
  • Argininosuccinate synthetase deficiency
  • Citrullinurias
  • Citrullinemia, subacute type
  • Late-onset citrullinemia type I
  • Neonatal metabolic acidemia
  • Citrullinaemia type 1
  • Argininosuccinic Acid Synthetase Deficiency Disease
  • Citrullinemia type I
  • Late-onset citrullinaemia type I
  • Citrullinaemia, subacute type
  • arginosuccinate synthetase deficiency
  • ARGININOSUCCINIC ACID SYNTHETASE DEFIC DIS
  • Argininosuccinic Acid Synthase Deficiency Disease
  • Solute carrier family 25 member 13 related citrin deficiency
  • ASS deficiency
  • Citrullinaemia type II
  • Argininosuccinate Synthase Deficiency Disease
  • CITRULLINURIA
  • ASS Deficiencies
  • DEFIC DIS ARGININOSUCCINATE SYNTHASE
  • Deficiency, Argininosuccinate Synthetase
  • DEFIC DIS ARGININOSUCCINIC ACID SYNTHASE
  • ASS1-gene related citrullinaemia type I
  • Late-onset citrullinemia type 1
  • Argininosuccinic Acid Synthetase Deficiency
  • Deficiency Disease, Argininosuccinic Acid Synthase
  • Deficiency, ASS
  • Citrullinemia (disorder)
  • Argininosuccinate Synthetase Deficiencies
  • Citrullinemia type II
  • Deficiency of argininosuccinate synthase (disorder)
  • ASS1-gene related citrullinemia type I
  • Adult onset type 2 citrullinaemia
  • Adult onset citrin deficiency
  • Adult onset type 2 citrullinemia
  • Deficiency of citrulline-aspartate ligase
  • Citrullinemia type 1
  • Citrin deficiency
  • ARGININOSUCCINATE SYNTHASE DEFIC DIS
  • Argininosuccinate synthase 1-gene related citrullinaemia type I
  • Citrullinaemia
  • Deficiencies, Argininosuccinate Synthetase
  • Citrullinaemia, neonatal type
  • Classic citrullinemia
  • Citrullinaemia type I
  • CIT
  • Argininosuccinate synthase 1-gene related citrullinemia type I
  • Argininosuccinate synthase deficiency
  • SLC25A13 related citrin deficiency
  • ARGININOSUCCINIC ACID SYNTHASE DEFIC DIS
  • Citrullinemias
  • Deficiency of argininosuccinate synthase
  • Neonatal metabolic acidaemia
  • Citrullinemia, neonatal type
  • Deficiency Disease, Argininosuccinate Synthase
  • Late-onset citrullinaemia type 1
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.

How does E72.23 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like citrullinemia affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E72.23?

There is no direct ICD-11 mapping available for E72.23 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.