E71.19
BillableOther disorders of branched-chain amino-acid metabolism
Other disorders of branched-chain amino-acid metabolism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hyperleucine-isoleucinemia
- Hypervalinemia
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
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hyperleucine-isoleucinaemia7046009
- Hyperleucine-isoleucinemia7046009
- 3-Methylcrotonyl-CoA carboxylase deficiency13144005
- BMCC deficiency13144005
- MCC deficiency13144005
- Methylcrotonyl-CoA carboxylase deficiency13144005
- Methylcrotonyl-coenzyme A carboxylase deficiency13144005
- beta-Methylcrotonylglycinuria, type 113144005
- Hyperleucinaemia24013007
- Hyperleucinemia24013007
- Leucine sensitivity24013007
- Leucinosis24013007
- Hyperaminoaciduria42930003
- Inborn error of amino acid metabolism42930003
- Autism, childhood onset43614003
- Autistic disorder of childhood onset43614003
- Childhood autism43614003
- Hypervalinaemia47719001
- Hypervalinemia47719001
- Valinaemia47719001
- Valine transaminase deficiency47719001
- Valinemia47719001
- Intermittent branched-chain ketonuria52270006
- Leucine-induced hypoglycaemia62151007
- Leucine-induced hypoglycemia62151007
- 3-Ketothiolase deficiency124258007
- 3-Methylhydroxybutyric acidaemia124258007
- 3-Methylhydroxybutyric acidemia124258007
- Acetoacetyl-CoA thiolase deficiency124258007
- Deficiency of acetoacetyl-CoA thiolase124258007
- Deficiency of acetyl-CoA acetyltransferase124258007
- Deficiency of acetyl-coenzyme A acetyltransferase124258007
- alpha-Methylacetoacetic aciduria124258007
- Deficiency of leucine aminotransferase124288003
- Deficiency of leucine-tRNA ligase124691008
- Deficiency of leucine-transfer ribonucleic acid ligase124691008
- Deficiency of leucyl-tRNA synthetase124691008
- Deficiency of isoleucine-tRNA ligase124692001
- Deficiency of isoleucine-transfer ribonucleic acid ligase124692001
- Deficiency of isoleucyl-tRNA synthetase124692001
- Deficiency of valine-tRNA ligase124695004
- Deficiency of valine-transfer ribonucleic acid ligase124695004
- Deficiency of valyl-tRNA synthetase124695004
- Isoleucinosis190701006
- Valinosis237944004
- Beta-ketothiolase deficiency237953006
- Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated237953006
- 3-Hydroxyisobutyric aciduria237957007
- Clinical manifestation of enzyme deficiency410053003
- 3-hydroxy-3-methylglutaric aciduria410059004
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency410059004
- HMG-CoA lyase deficiency410059004
- Hydroxymethylglutaric aciduria410059004
- Disorder of isoleucine metabolism444755001
- Disorder of valine metabolism444756000
- Isobutyrylglycinuria445571008
- CMAMMA - combined malonic and methylmalonic aciduria702365002
- Combined malonic and methylmalonic aciduria702365002
- Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency771448004
- Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency782828005
- Developmental delay due to MMSDH (methylmalonate semialdehyde dehydrogenase) deficiency782828005
- Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency782828005
- ACAD8-gene related deficiency of isobutyryl-coenzyme A dehydrogenase1306747001
- Isobutyric aciduria1306747001
- Isobutyryl-CoA dehydrogenase deficiency disease1306747001
- Isobutyryl-coenzyme A dehydrogenase deficiency disease1306747001
- 2-methylbutyric aciduria1306751004
- 2-methylbutyryl-coenzyme A dehydrogenase deficiency disease1306751004
- ACADSB-gene related deficiency of 2-methylbutyryl-coenzyme A dehydrogenase1306751004
- Short/branched-chain acyl-coA dehydrogenase deficiency disease1306751004
UMLS
- HYPERLEUCINE-ISOLEUCINEMIAC0268574
- Hyperleucine-IsoleucinemiaC0268574
- Hyperleucine-isoleucinaemiaC0268574
- Hyperleucine-isoleucinemiaC0268574
- Hyperleucine-isoleucinemia (disorder)C0268574
- HYPERVALINEMIAC0268573
- High blood valine concentrationC0268573
- HypervalinaemiaC0268573
- HypervalinemiaC0268573
- Hypervalinemia (disorder)C0268573
- VALINE TRANSAMINASE DEFICIENCYC0268573
- VALINEMIAC0268573
- ValinaemiaC0268573
- Valine transaminase deficiencyC0268573
- ValinemiaC0268573
- hypervalinemiaC0268573
- valinemiaC0268573
- Other disorders of branched-chain amino-acid metabolismC0348484
Frequently Asked Questions
What is the ICD-10 code for other disorders of branched-chain amino-acid metabolism?
The ICD-10-CM code for other disorders of branched-chain amino-acid metabolism is E71.19. The full clinical description is "Other disorders of branched-chain amino-acid metabolism". E71.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.19 mean?
ICD-10-CM code E71.19 represents "Other disorders of branched-chain amino-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 E71.19 a billable code?
Yes, E71.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.19 in?
E71.19 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.19?
E71.19 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 3 more.
What SNOMED CT codes does E71.19 map to?
E71.19 maps to 27 SNOMED CT concepts: 1306751004, 237957007, 124258007, 13144005, 410059004, and 22 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.19?
E71.19 is linked to 3 UMLS Concept Unique Identifiers: C0268574, C0268573, C0348484. 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.