E78.71
BillableBarth syndrome
Barth syndrome
Coding Notes
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)
- sphingolipidosis (E75.0-E75.3)
- Niemann-Pick disease type C (E75.242)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
UMLS
- 3 Methylglutaconic Aciduria, Type IIC0574083
- 3 Methylglutaconicaciduria Type 2C0574083
- 3 methylglutaconic aciduria, type IIC0574083
- 3-METHYLGLUTACONIC ACIDURIA, TYPE IIC0574083
- 3-Methylglutaconic Aciduria Type 2C0574083
- 3-Methylglutaconic Aciduria, Type IIC0574083
- 3-Methylglutaconic aciduria type 2C0574083
- 3-Methylglutaconic aciduria type 2 (disorder)C0574083
- 3-Methylglutaconicaciduria Type 2C0574083
- 3-Methylglutaconicaciduria Type 2sC0574083
- 3-Methylglutaconicaciduria Type IIC0574083
- 3-Methylglutaconicaciduria Type IIsC0574083
- 3-methylglutaconic aciduria type 2C0574083
- BARTH SYNDROMEC0574083
- BTHSC0574083
- Barth SyndromeC0574083
- Barth syndromeC0574083
- CARDIOSKELETAL MYOPATHY WITH NEUTROPENIA AND ABNORMAL MITOCHONDRIAC0574083
- Cardioskeletal Myopathy with Neutropenia and Abnormal MitochondriaC0574083
- Cardioskeletal myopathy with neutropenia and abnormal mitochondriaC0574083
- DNAJC19 defectC0574083
- MGA Type 2C0574083
- MGA Type 2sC0574083
- MGA Type IIC0574083
- MGA Type IIsC0574083
- MGA type 2C0574083
- MGA type IIC0574083
- MGA, TYPE IIC0574083
- MGA2C0574083
- MGCA2C0574083
- Syndrome, BarthC0574083
- Type 2, 3-MethylglutaconicaciduriaC0574083
- Type 2, MGAC0574083
- Type 2s, MGAC0574083
- Type II, MGAC0574083
- Type IIs, MGAC0574083
- barth syndromeC0574083
- barths syndromeC0574083
Frequently Asked Questions
What is the ICD-10 code for barth syndrome?
The ICD-10-CM code for barth syndrome is E78.71. The full clinical description is "Barth syndrome". E78.71 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.71 mean?
ICD-10-CM code E78.71 represents "Barth syndrome". 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 E78.71 a billable code?
Yes, E78.71 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.71 in?
E78.71 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.71?
E78.71 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 5 more.
What SNOMED CT codes does E78.71 map to?
E78.71 maps to 1 SNOMED CT concept: 297231002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.71?
E78.71 is linked to 1 UMLS Concept Unique Identifier: C0574083. 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.