E71.121
BillablePropionic acidemia
Propionic acidemia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(2)
Also Known As / Clinical Terms(122)
SNOMED CT
- Hyperglycinaemia with ketosis and leucopenia69080001
- Hyperglycinemia with ketosis and leukopenia69080001
- Ketotic glycinaemia69080001
- Ketotic glycinemia69080001
- Ketotic hyperglycinaemia69080001
- Ketotic hyperglycinemia69080001
- PCC - Propionyl-CoA carboxylase deficiency69080001
- Propionic acidaemia69080001
- Propionic acidemia69080001
- Propionic aciduria69080001
- Propionyl-CoA carboxylase deficiency69080001
- Deficiency of propionyl-CoA carboxylase124718009
- Deficiency of propionyl-coenzyme A carboxylase124718009
- PCCA-gene related propionyl-coenzyme A carboxylase deficiency pccA complementation group303094000
- Propionyl-CoA carboxylase deficiency pccA complementation group303094000
- Propionyl-coenzyme A carboxylase deficiency pccA complementation group303094000
- PCCB-gene related propionyl-coenzyme A carboxylase deficiency pccBC complementation group303095004
- Propionyl-CoA carboxylase deficiency pccBC complementation group303095004
- Propionyl-coenzyme A carboxylase deficiency pccBC complementation group303095004
- Propionic acidaemia, type I399087009
- Propionic acidemia, type I399087009
- Propionic acidaemia, type II399149003
- Propionic acidemia, type II399149003
UMLS
- Acidemia PropionicC0268579
- Acidemia PropionicsC0268579
- Acidemia, PropionicC0268579
- Carboxylase Deficiencies, Propionyl-CoAC0268579
- Carboxylase Deficiency, Propionyl-CoAC0268579
- Deficiencies, Propionyl-CoA CarboxylaseC0268579
- Deficiency, PCCC0268579
- Deficiency, Propionyl-CoA CarboxylaseC0268579
- GLYCINEMIA, KETOTICC0268579
- Glycinemia, KetoticC0268579
- Glycinemias, KetoticC0268579
- HYPERGLYCINEMIA WITH KETOACIDOSIS AND LEUKOPENIAC0268579
- Hyperglycinaemia with ketosis and leucopeniaC0268579
- Hyperglycinemia With Ketoacidosis And LeukopeniaC0268579
- Hyperglycinemia with ketoacidosis and leukopeniaC0268579
- Hyperglycinemia with ketosis and leukopeniaC0268579
- Hyperglycinemia, KetoticC0268579
- Hyperglycinemias, KetoticC0268579
- KETOTIC HYPERGLYCINEMIAC0268579
- Ketotic GlycinemiaC0268579
- Ketotic GlycinemiasC0268579
- Ketotic HyperglycinemiaC0268579
- Ketotic HyperglycinemiasC0268579
- Ketotic glycinaemiaC0268579
- Ketotic glycinemiaC0268579
- Ketotic hyperglycinaemiaC0268579
- Ketotic hyperglycinemiaC0268579
- PCC - Propionyl-CoA carboxylase deficiencyC0268579
- PCC DeficienciesC0268579
- PCC DeficiencyC0268579
- PCC deficiencyC0268579
- PROPC0268579
- PROPIONIC ACIDEMIAC0268579
- Propionic AcidemiaC0268579
- Propionic AcidemiasC0268579
- Propionic acidaemiaC0268579
- Propionic acidemiaC0268579
- Propionic acidemia (disorder)C0268579
- Propionic aciduriaC0268579
- Propionic, AcidemiaC0268579
- PropionicacidemiaC0268579
- PropionicacidemiasC0268579
- Propionyl CoA Carboxylase DeficiencyC0268579
- Propionyl-CoA Carboxylase DeficienciesC0268579
- Propionyl-CoA Carboxylase DeficiencyC0268579
- Propionyl-CoA carboxylase deficiencyC0268579
- ketotic glycinemiaC0268579
- ketotic hyperglycinaemiaC0268579
- ketotic hyperglycinemiaC0268579
- propionic acidaemiaC0268579
- propionic acidemiaC0268579
- propionyl coA carboxylase deficiencyC0268579
Clinical Terms
- Propionyl-CoA carboxylase deficiency pccBC complementation group
- Acidemia, Propionic
- Deficiency, PCC
- propionic acidaemia
- propionyl coA carboxylase deficiency
- Propionic aciduria
- Deficiencies, Propionyl-CoA Carboxylase
- GLYCINEMIA, KETOTIC
- Ketotic hyperglycinaemia
- Propionyl-CoA carboxylase deficiency
- Propionyl-coenzyme A carboxylase deficiency pccBC complementation group
- Hyperglycinemias, Ketotic
- Propionic, Acidemia
- PCCB-gene related propionyl-coenzyme A carboxylase deficiency pccBC complementation group
- Ketotic Hyperglycinemia
- Carboxylase Deficiencies, Propionyl-CoA
- Acidemia Propionics
- Propionyl-CoA Carboxylase Deficiencies
- PCC deficiency
- PCCA-gene related propionyl-coenzyme A carboxylase deficiency pccA complementation group
- HYPERGLYCINEMIA WITH KETOACIDOSIS AND LEUKOPENIA
- PCC Deficiencies
- Propionicacidemias
- Propionicacidemia
- ketotic glycinemia
- Deficiency, Propionyl-CoA Carboxylase
- Propionyl-coenzyme A carboxylase deficiency pccA complementation group
- Deficiency of propionyl-CoA carboxylase
- Ketotic glycinaemia
- Carboxylase Deficiency, Propionyl-CoA
- Propionyl-CoA carboxylase deficiency pccA complementation group
- Propionic acidemia (disorder)
- Propionic acidemia, type II
- Propionic acidaemia, type I
- Hyperglycinaemia with ketosis and leucopenia
- PROP
- Propionic acidemia, type I
- Hyperglycinemia, Ketotic
- Deficiency of propionyl-coenzyme A carboxylase
- Hyperglycinemia with ketosis and leukopenia
- Glycinemias, Ketotic
- Ketotic Glycinemias
- Propionic acidaemia, type II
- Ketotic Hyperglycinemias
- Propionic Acidemias
- Acidemia Propionic
- PCC - Propionyl-CoA carboxylase deficiency
Frequently Asked Questions
What is the ICD-10 code for propionic acidemia?
The ICD-10-CM code for propionic acidemia is E71.121. The full clinical description is "Propionic acidemia". E71.121 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.121 mean?
ICD-10-CM code E71.121 represents “Propionic 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 E71.121 a billable code?
Yes, E71.121 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.121 in?
E71.121 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.121?
E71.121 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 E71.121 map to?
E71.121 maps to 6 SNOMED CT concepts: 124718009, 69080001, 303094000, 303095004, 399087009, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.121?
E71.121 is linked to 1 UMLS Concept Unique Identifier: C0268579. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E71.121 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like propionic 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 E71.121?
There is no direct ICD-11 mapping available for E71.121 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.