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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
Related Codes(1)
Also Known As / Clinical Terms(88)
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
Clinical Terms
- Succinate-semialdehyde dehydrogenase deficiency (disorder)
- 4-Hydroxybutyricaciduria
- Disorders of GABA metabolism
- GABA metabolic defect
- Gamma-Hydroxybutyric Acidemia
- Gamma-Hydroxybutyric Aciduria
- Gamma-aminobutyric acid transaminase deficiency (disorder)
- succinic semialdehyde dehydrogenase deficiency
- GABA transaminase deficiency
- 4-hydroxybutyric aciduria
- Gamma-aminobutyrate transaminase deficiency
- SSADH (succinic semialdehyde dehydrogenase) deficiency
- GABA-T deficiency
- SSADH deficiency
- GABA transferase deficiency
- succinate-semialdehyde dehydrogenase deficiency
- Disorder of the gamma-glutamyl cycle
- Disorder of GABA (gamma aminobutyric acid) metabolism
- GABA-transaminase deficiency
- 4 hydroxybutyric aciduria
- Disorder of gamma-glutamyl cycle
- ABAT deficiency
- GABATD
- Gamma-aminobutyric acid transaminase deficiency
- Gamma-hydroxybutyric acidaemia
- Gamma aminobutyric acid transaminase deficiency
- Gamma aminobutyrate transaminase deficiency
- SSADHD
- 4 alpha aminobutyrate transaminase deficiency
- Disorder of beta and omega amino acid metabolism
- GABAuria
- Disorder of gamma-aminobutyric acid metabolism (disorder)
- Disorder of gamma aminobutyric acid metabolism
- Disorder of gamma-aminobutyric acid metabolism
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.
How does E72.81 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of gamma aminobutyric acid metabolism 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 E72.81?
There is no direct ICD-11 mapping available for E72.81 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.