E71.313
BillableGlutaric aciduria type II
Glutaric aciduria type II
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Glutaric aciduria type II A
- Glutaric aciduria type II B
- Glutaric aciduria type II C
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)
- peroxisomal disorders (E71.5)
- Refsum's disease (G60.1)
- Schilder's disease (G37.0)
- glutaric aciduria (type 1) NOS (E72.3)
Also Known As / Clinical Terms
SNOMED CT
- Ethylmalonic-adipicaciduria22886006
- Glutaric acidaemia, type 222886006
- Glutaric acidemia, type 222886006
- Glutaric aciduria type II22886006
- Glutaric aciduria, type 222886006
- MAD - Multiple acyl-CoA dehydrogenase deficiency22886006
- MADD - multiple acyl-CoA dehydrogenase deficiency22886006
- Glutaric aciduria28987007
- Electron transfer flavoprotein-ubiquinone oxidoreductase deficiency1187534001
- Beta chain electron transfer flavoprotein deficiency1187541007
- Alpha chain electron transfer flavoprotein deficiency1187542000
UMLS
- Aciduria, Ethylmalonic-AdipicC0268596
- Acidurias, Ethylmalonic-AdipicC0268596
- EMAC0268596
- ETHYLMALONIC-ADIPICACIDURIAC0268596
- Electron Transfer Flavoprotein DeficiencyC0268596
- Electron transfer flavoprotein deficiencyC0268596
- Ethylmalonic Adipic AciduriaC0268596
- Ethylmalonic AdipicaciduriaC0268596
- Ethylmalonic-Adipic AciduriaC0268596
- Ethylmalonic-Adipic AciduriasC0268596
- Ethylmalonic-AdipicaciduriaC0268596
- Ethylmalonic-adipicaciduriaC0268596
- GA IIC0268596
- GA2C0268596
- GLUTARIC ACIDEMIA IIC0268596
- GLUTARIC ACIDURIA IIC0268596
- Glutaric Acidemia Type 2C0268596
- Glutaric Acidemia Type IIC0268596
- Glutaric Acidemia, Type 2C0268596
- Glutaric Aciduria IIC0268596
- Glutaric Aciduria Type 2C0268596
- Glutaric Aciduria Type IIC0268596
- Glutaric Aciduria, Type 2C0268596
- Glutaric acidaemia, type 2C0268596
- Glutaric acidemia type IIC0268596
- Glutaric acidemia, type 2C0268596
- Glutaric aciduria type IIC0268596
- Glutaric aciduria, type 2C0268596
- Glutaric aciduria, type 2 (disorder)C0268596
- MADC0268596
- MAD - Multiple acyl-CoA dehydrogenase deficiencyC0268596
- MADDC0268596
- MADD (Multiple Acyl CoA Dehydrogenase Deficiency)C0268596
- MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)C0268596
- MADD - multiple acyl-CoA dehydrogenase deficiencyC0268596
- MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)C0268596
- MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCYC0268596
- Multiple Acyl CoA Dehydrogenase DeficiencyC0268596
- Multiple Acyl Coenzyme A Dehydrogenase DeficiencyC0268596
- Multiple Acyl-CoA Dehydrogenase DeficiencyC0268596
- Multiple FAD Dehydrogenase DeficiencyC0268596
- Multiple FAD dehydrogenase deficiencyC0268596
- Multiple acyl-CoA dehydrogenase deficiencyC0268596
- Multiple acyl-coenzyme A dehydrogenase deficiencyC0268596
- emaC0268596
- glutaric acidemia type 2C0268596
- Glutaric aciduria type II AC2874240
- Glutaric aciduria type II BC2874241
- Glutaric aciduria type II CC2874242
Frequently Asked Questions
What is the ICD-10 code for glutaric aciduria type ii?
The ICD-10-CM code for glutaric aciduria type ii is E71.313. The full clinical description is "Glutaric aciduria type II". E71.313 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.313 mean?
ICD-10-CM code E71.313 represents "Glutaric aciduria type II". 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 E71.313 a billable code?
Yes, E71.313 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.313 in?
E71.313 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.313?
E71.313 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 7 more.
What SNOMED CT codes does E71.313 map to?
E71.313 maps to 5 SNOMED CT concepts: 1187542000, 1187541007, 1187534001, 22886006, 28987007. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.313?
E71.313 is linked to 4 UMLS Concept Unique Identifiers: C0268596, C2874240, C2874241, C2874242. 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.