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 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)
- histiocytosis X (chronic) (C96.6)
- monoclonal gammopathy (of undetermined significance) (D47.2)
- polyclonal hypergammaglobulinemia (D89.0)
- Waldenström macroglobulinemia (C88.00)
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
Also Known As / Clinical Terms
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
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 you should also code: 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.
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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.