D82.8
BillableImmunodeficiency associated with oth major defects
Immunodeficiency associated with other specified major defects
Coding Notes
Includes
Conditions included under this code
- defects in the complement system
- immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
- sarcoidosis
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- HAE - Hereditary angio-oedema82966003
- HAE - Hereditary angioedema82966003
- HANE - Hereditary angioneurotic edema82966003
- HANE - Hereditary angioneurotic oedema82966003
- Hereditary Quincke's edema82966003
- Hereditary Quincke's oedema82966003
- Hereditary angio-oedema82966003
- Hereditary angioedema82966003
- Hereditary angioneurotic edema82966003
- Hereditary angioneurotic oedema82966003
- 18-p syndrome with associated immunodeficiency234640004
- Immunodeficiency associated with 18p syndrome234640004
- Hereditary angio-oedema with normal C1 esterase inhibitor activity427167008
- Hereditary angioedema - type 3427167008
- Hereditary angioedema with normal C1 esterase inhibitor activity427167008
- Hereditary angioneurotic edema with normal C1 esterase inhibitor activity427167008
- Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity427167008
- Primary immunodeficiency syndrome due to p14 deficiency718717004
- Primary immunodeficiency syndrome with short stature718717004
- Woods Black Norbury syndrome719827008
- X-linked immunoneurologic disorder719827008
Frequently Asked Questions
What is ICD-10 code D82.8?
ICD-10-CM code D82.8 represents "Immunodeficiency associated with other specified major defects". It is a billable/specific code that can be used on a claim.
Is D82.8 a billable code?
Yes, D82.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D82.8 in?
D82.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D82.8?
D82.8 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease (systemic) NOS (M35.9); functional disorders of polymorphonuclear neutrophils (D71); human immunodeficiency virus [HIV] disease (B20); and 1 more.
What SNOMED CT codes does D82.8 map to?
D82.8 maps to 5 SNOMED CT concepts: 234640004, 82966003, 427167008, 718717004, 719827008. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D82.8?
D82.8 is linked to 1 UMLS Concept Unique Identifier: C0477325. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.