E88.01
BillableAlpha-1-antitrypsin deficiency
Alpha-1-antitrypsin deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- AAT deficiency
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •histiocytosis X (chronic)C96.6
- •monoclonal gammopathy (of undetermined significance)D47.2
- •polyclonal hypergammaglobulinemiaD89.0
- •Waldenström macroglobulinemiaC88.00
Excludes 2
Conditions not included here, but the patient may have both
Use Additional Code
Additional codes that should follow this code
- codes for associated conditions
Related Codes(2)
Also Known As / Clinical Terms(58)
SNOMED CT
- Alpha-1-antitrypsin deficiency30188007
- alpha-1-Proteinase inhibitor deficiency30188007
- Alpha-1-antitrypsin hepatitis190944000
- Pulmonary emphysema in alpha-1 PI deficiency233674008
- Pulmonary emphysema in alpha-1 primary immunodeficiency deficiency233674008
- Panniculitis due to action of lipolytic enzymes402687009
- Alpha-1 anti-trypsin deficiency panniculitis403415009
- Panniculitis due to alpha-1 anti-trypsin deficiency403415009
UMLS
- 1 alpha antitrypsin deficiencyC0221757
- A-1ATDC0221757
- A1ADC0221757
- A1ATDC0221757
- AATC0221757
- AAT deficiencyC0221757
- AATDC0221757
- ALPHA 1 ANTITRYPSIN DEFICC0221757
- ALPHA-1-ANTITRYPSIN DEFICIENCYC0221757
- Alpha-1 Antitrypsin DeficiencyC0221757
- Alpha-1 anti-trypsin deficiencyC0221757
- Alpha-1 antitrypsin deficiencyC0221757
- Alpha-1 proteinase inhibitor deficiencyC0221757
- Alpha-1-antitrypsin deficiencyC0221757
- Alpha-1-antitrypsin deficiency (disorder)C0221757
- Deficiencies, alpha 1-AntitrypsinC0221757
- Deficiency, alpha 1-AntitrypsinC0221757
- alpha 1 Antitrypsin DeficiencyC0221757
- alpha 1 antitrypsin deficiencyC0221757
- alpha 1-Antitrypsin DeficienciesC0221757
- alpha 1-Antitrypsin DeficiencyC0221757
- alpha 1-antitrypsin deficiencyC0221757
- alpha-1 anti-trypsin deficiencyC0221757
- alpha-1 antitrypsin deficiencyC0221757
- alpha-1-Proteinase inhibitor deficiencyC0221757
- alpha-1-antitrypsin deficiencyC0221757
Clinical Terms
- alpha 1-Antitrypsin Deficiencies
- AAT
- alpha-1 anti-trypsin deficiency
- Panniculitis due to alpha-1 anti-trypsin deficiency
- Panniculitis due to action of lipolytic enzymes
- Alpha-1-antitrypsin hepatitis
- Alpha-1 Antitrypsin Deficiency
- AATD
- Deficiencies, alpha 1-Antitrypsin
- Alpha-1 proteinase inhibitor deficiency
- A1ATD
- alpha-1-Proteinase inhibitor deficiency
- A1AD
- alpha 1 antitrypsin deficiency
- Alpha-1 anti-trypsin deficiency panniculitis
- alpha 1-antitrypsin deficiency
- 1 alpha antitrypsin deficiency
- Alpha-1-antitrypsin deficiency (disorder)
- A-1ATD
- ALPHA 1 ANTITRYPSIN DEFIC
- Deficiency, alpha 1-Antitrypsin
- Pulmonary emphysema in alpha-1 PI deficiency
- Pulmonary emphysema in alpha-1 primary immunodeficiency deficiency
- AAT deficiency
Frequently Asked Questions
What is the ICD-10 code for alpha-1-antitrypsin deficiency?
The ICD-10-CM code for alpha-1-antitrypsin deficiency is E88.01. The full clinical description is "Alpha-1-antitrypsin deficiency". E88.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E88.01 mean?
ICD-10-CM code E88.01 represents “Alpha-1-antitrypsin deficiency”. 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 E88.01 a billable code?
Yes, E88.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E88.01 in?
E88.01 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E88.01?
E88.01 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.
Are additional codes required with E88.01?
Yes, when using E88.01, also report: codes for associated conditions.
What SNOMED CT codes does E88.01 map to?
E88.01 maps to 5 SNOMED CT concepts: 403415009, 30188007, 190944000, 402687009, 233674008. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E88.01?
E88.01 is linked to 1 UMLS Concept Unique Identifier: C0221757. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E88.01 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like alpha-1-antitrypsin deficiency 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 E88.01?
There is no direct ICD-11 mapping available for E88.01 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.