E71.120
BillableMethylmalonic acidemia
Methylmalonic acidemia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(2)
Also Known As / Clinical Terms(140)
SNOMED CT
- Adenosylcobalamin and methylcobalamin synthesis defect4409006
- Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis4409006
- Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis4409006
- Homocystinuria11282001
- CblD - Cobalamin locus D31220004
- CblD methylmalonic acidaemia and homocystinuria31220004
- CblD methylmalonic acidemia and homocystinuria31220004
- Cobalamin D disease31220004
- M0E.321 Cobalamin locus D variant31220004
- MMA - Methylmalonic aciduria42393006
- Methylmalonic acidaemia42393006
- Methylmalonic acidemia42393006
- Adenosylcobalamin synthesis defect69614003
- Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis69614003
- Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis69614003
- Methylmalonic aciduria, type II69614003
- Vitamin B12-responsive methylmalonic acidaemia69614003
- Vitamin B12-responsive methylmalonic acidemia69614003
- CblA - Cobalamin locus A73843004
- CblA methylmalonic acidaemia73843004
- CblA methylmalonic acidemia73843004
- Cobalamin A disease73843004
- Cobalamin locus A variant73843004
- CblC - Cobalamin locus C74653006
- CblC methylmalonic acidaemia and homocystinuria74653006
- CblC methylmalonic acidemia and homocystinuria74653006
- Cobalamin C disease74653006
- Cobalamin locus C variant74653006
- CblF - Cobalamin locus F variant80887004
- CblF methylmalonic acidaemia and homocystinuria80887004
- CblF methylmalonic acidemia and homocystinuria80887004
- Cobalamin locus F variant80887004
- Inherited methylmalonic acidaemia AND homocystinuria80887004
- Inherited methylmalonic acidemia AND homocystinuria80887004
- CblB - Cobalamin locus B82245003
- CblB methylmalonic acidaemia82245003
- CblB methylmalonic acidemia82245003
- Cobalamin B disease82245003
- Cobalamin locus B variant82245003
- Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria715338007
- Fatal infantile lactic acidosis with methylmalonic aciduria715338007
- MCEE-gene related methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency765137006
- MCEE-gene related methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency765137006
- Methylmalonic acidaemia due to methylmalonyl-CoA epimerase deficiency765137006
- Methylmalonic acidaemia due to methylmalonyl-CoA racemase deficiency765137006
- Methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency765137006
- Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency765137006
- Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency765137006
- Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency765137006
- Mitochondrial DNA depletion syndrome encephalomyopathic form765401006
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form765401006
- Methylmalonic acidaemia TCb1R type771444002
- Methylmalonic acidemia TCb1R type771444002
- Methylmalonic aciduria due to transcobalamin receptor defect771444002
- Booth Haworth Dilling syndrome1197052008
- Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria1197052008
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria1197052008
- Mitochondrial encephalomyopathy aminoacidopathy syndrome1197052008
- mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome encephalomyopathic form with methylmalonic aciduria1197052008
UMLS
- Acidemia, methylmalonicC0268583
- Elevated circulating methylmalonic acid concentrationC0268583
- Isolated Methylmalonic AcidemiaC0268583
- Isolated methylmalonic acidemiaC0268583
- MMAC0268583
- MMA - Methylmalonic aciduriaC0268583
- Methylmalonic AcidemiaC0268583
- Methylmalonic AciduriaC0268583
- Methylmalonic acidaemiaC0268583
- Methylmalonic acidemiaC0268583
- Methylmalonic acidemia (disorder)C0268583
- Methylmalonic aciduriaC0268583
- acidemias methylmalonicC0268583
- methylmalonic acidaemiaC0268583
- methylmalonic acidemiaC0268583
- methylmalonic aciduriaC0268583
Clinical Terms
- Cobalamin locus B variant
- Methylmalonic acidaemia due to methylmalonyl-CoA racemase deficiency
- Vitamin B12-responsive methylmalonic acidaemia
- CblD - Cobalamin locus D
- MCEE-gene related methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency
- Methylmalonic Aciduria
- Cobalamin C disease
- Acidemia, methylmalonic
- CblC methylmalonic acidaemia and homocystinuria
- Methylmalonic acidemia (disorder)
- Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency
- Isolated methylmalonic acidemia
- Booth Haworth Dilling syndrome
- Methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency
- Inherited methylmalonic acidaemia AND homocystinuria
- CblB - Cobalamin locus B
- CblB methylmalonic acidaemia
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
- Cobalamin locus A variant
- Cobalamin A disease
- CblF - Cobalamin locus F variant
- Cobalamin B disease
- CblF methylmalonic acidaemia and homocystinuria
- Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria
- Adenosylcobalamin and methylcobalamin synthesis defect
- Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis
- Methylmalonic aciduria due to transcobalamin receptor defect
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria
- CblA - Cobalamin locus A
- MMA
- acidemias methylmalonic
- CblC methylmalonic acidemia and homocystinuria
- Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria
- CblC - Cobalamin locus C
- Homocystinuria
- Fatal infantile lactic acidosis with methylmalonic aciduria
- Mitochondrial encephalomyopathy aminoacidopathy syndrome
- Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis
- Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis
- Methylmalonic aciduria, type II
- CblD methylmalonic acidaemia and homocystinuria
- CblA methylmalonic acidaemia
- CblF methylmalonic acidemia and homocystinuria
- Adenosylcobalamin synthesis defect
- Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency
- Cobalamin locus C variant
- Cobalamin locus F variant
- mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome encephalomyopathic form with methylmalonic aciduria
- Mitochondrial DNA depletion syndrome encephalomyopathic form
- MCEE-gene related methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency
- methylmalonic acidaemia
- Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency
- MMA - Methylmalonic aciduria
- Methylmalonic acidaemia due to methylmalonyl-CoA epimerase deficiency
- Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis
- Methylmalonic acidaemia TCb1R type
- Inherited methylmalonic acidemia AND homocystinuria
- CblD methylmalonic acidemia and homocystinuria
- Methylmalonic acidemia TCb1R type
- Cobalamin D disease
- Elevated circulating methylmalonic acid concentration
- Vitamin B12-responsive methylmalonic acidemia
- M0E.321 Cobalamin locus D variant
- CblB methylmalonic acidemia
- CblA methylmalonic acidemia
Frequently Asked Questions
What is the ICD-10 code for methylmalonic acidemia?
The ICD-10-CM code for methylmalonic acidemia is E71.120. The full clinical description is "Methylmalonic acidemia". E71.120 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.120 mean?
ICD-10-CM code E71.120 represents “Methylmalonic acidemia”. 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 E71.120 a billable code?
Yes, E71.120 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.120 in?
E71.120 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.120?
E71.120 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 E71.120 map to?
E71.120 maps to 14 SNOMED CT concepts: 4409006, 69614003, 1197052008, 73843004, 82245003, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.120?
E71.120 is linked to 1 UMLS Concept Unique Identifier: C0268583. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E71.120 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like methylmalonic acidemia 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 E71.120?
There is no direct ICD-11 mapping available for E71.120 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.