E72.81
BillableDisorders of gamma aminobutyric acid metabolism
Disorders of gamma aminobutyric acid metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 4-hydroxybutyric aciduria
- Disorders of GABA metabolism
- GABA metabolic defect
- GABA transaminase deficiency
- GABA-T deficiency
- Gamma-hydroxybutyric aciduria
- SSADHD
- Succinic semialdehyde dehydrogenase 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.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Disorder of gamma-glutamyl cycle9128006
- Disorder of the gamma-glutamyl cycle9128006
- Disorder of beta and omega amino acid metabolism237940008
- Gamma-aminobutyric acid transaminase deficiency237941007
- Disorder of GABA (gamma aminobutyric acid) metabolism16909721000119103
- Disorder of gamma aminobutyric acid metabolism16909721000119103
- Disorder of gamma-aminobutyric acid metabolism16909721000119103
UMLS
- 4 alpha aminobutyrate transaminase deficiencyC0342708
- ABAT deficiencyC0342708
- GABA transaminase deficiencyC0342708
- GABA transferase deficiencyC0342708
- GABA-T deficiencyC0342708
- GABA-TRANSAMINASE DEFICIENCYC0342708
- GABA-transaminase deficiencyC0342708
- GABATDC0342708
- Gaba-Transaminase DeficiencyC0342708
- Gamma aminobutyrate transaminase deficiencyC0342708
- Gamma aminobutyric acid transaminase deficiencyC0342708
- Gamma-aminobutyrate transaminase deficiencyC0342708
- Gamma-aminobutyric acid transaminase deficiencyC0342708
- Gamma-aminobutyric acid transaminase deficiency (disorder)C0342708
- 4 hydroxybutyric aciduriaC0268631
- 4-HYDROXYBUTYRIC ACIDURIAC0268631
- 4-Hydroxybutyric aciduriaC0268631
- 4-HydroxybutyricaciduriaC0268631
- 4-hydroxybutyric aciduriaC0268631
- GABA METABOLIC DEFECTC0268631
- GABA metabolic defectC0268631
- GABAuriaC0268631
- GAMMA-HYDROXYBUTYRIC ACIDURIAC0268631
- Gamma-Hydroxybutyric AcidemiaC0268631
- Gamma-Hydroxybutyric AciduriaC0268631
- Gamma-hydroxybutyric acidaemiaC0268631
- Gamma-hydroxybutyric acidemiaC0268631
- Gamma-hydroxybutyric aciduriaC0268631
- SSADH (succinic semialdehyde dehydrogenase) deficiencyC0268631
- SSADH DEFICIENCYC0268631
- SSADH DeficiencyC0268631
- SSADH deficiencyC0268631
- SSADHDC0268631
- SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCYC0268631
- Succinate-semialdehyde dehydrogenase deficiencyC0268631
- Succinate-semialdehyde dehydrogenase deficiency (disorder)C0268631
- Succinic Semialdehyde Dehydrogenase DeficiencyC0268631
- Succinic semialdehyde dehydrogenase deficiencyC0268631
- gamma-Hydroxybutyric aciduriaC0268631
- succinate-semialdehyde dehydrogenase deficiencyC0268631
- succinic semialdehyde dehydrogenase deficiencyC0268631
- Disorder of GABA (gamma aminobutyric acid) metabolismC4702813
- Disorder of gamma aminobutyric acid metabolismC4702813
- Disorder of gamma-aminobutyric acid metabolismC4702813
- Disorder of gamma-aminobutyric acid metabolism (disorder)C4702813
- Disorders of GABA metabolismC4702813
- Disorders of gamma aminobutyric acid metabolismC4702813
Frequently Asked Questions
What is the ICD-10 code for disorders of gamma aminobutyric acid metabolism?
The ICD-10-CM code for disorders of gamma aminobutyric acid metabolism is E72.81. The full clinical description is "Disorders of gamma aminobutyric acid metabolism". E72.81 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.81 mean?
ICD-10-CM code E72.81 represents "Disorders of gamma aminobutyric acid 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 E72.81 a billable code?
Yes, E72.81 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.81 in?
E72.81 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.81?
E72.81 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 9 more.
What SNOMED CT codes does E72.81 map to?
E72.81 maps to 4 SNOMED CT concepts: 16909721000119103, 237940008, 9128006, 237941007. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.81?
E72.81 is linked to 3 UMLS Concept Unique Identifiers: C0342708, C0268631, C4702813. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.