D89.82
BillableAutoimmune lymphoproliferative syndrome [ALPS]
Autoimmune lymphoproliferative syndrome [ALPS]
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) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •transplant failure and rejectionT86
Related Codes(4)
Also Known As / Clinical Terms(74)
SNOMED CT
- ALPS - autoimmune lymphoproliferative syndrome702444009
- Autoimmune lymphoproliferative syndrome702444009
- Canale-Smith syndrome702444009
- DALD - Dianzani autoimmune lymphoproliferative disease721093000
- Dianzani autoimmune lymphoproliferative disease721093000
- Autoimmune lymphoproliferative syndrome with recurrent viral infection722290008
- Caspase 8 deficiency syndrome722290008
- Autoimmune lymphoproliferative syndrome type 4723508002
- Autoimmune lymphoproliferative syndrome type IV723508002
- RALD - RAS-associated autoimmune leucoproliferative disease723508002
- RALD - RAS-associated autoimmune leukoproliferative disease723508002
- RAS-associated autoimmune leucoproliferative disease723508002
- RAS-associated autoimmune leukoproliferative disease723508002
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency1197361002
- Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency1197361002
- CTLA-4 haploinsufficiency with autoimmune infiltration disease1197361002
- STAT3-related early-onset multisystem autoimmune disease1197362009
- Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease1197362009
UMLS
- ALPSC1328840
- ALPS (autoimmune lymphoproliferative syndrome)C1328840
- ALPS - autoimmune lymphoproliferative syndromeC1328840
- AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROMEC1328840
- AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANTC1328840
- Autoimmune Lymphoproliferative SyndromeC1328840
- Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal DominantC1328840
- Autoimmune Lymphoproliferative SyndromesC1328840
- Autoimmune lymphoproliferative syndromeC1328840
- Autoimmune lymphoproliferative syndrome (disorder)C1328840
- Autoimmune lymphoproliferative syndrome [ALPS]C1328840
- CANALE-SMITH SYNDROMEC1328840
- Canale Smith SyndromeC1328840
- Canale-Smith SyndromeC1328840
- Canale-Smith SyndromesC1328840
- Canale-Smith syndromeC1328840
- Lymphoproliferative Syndrome, AutoimmuneC1328840
- Lymphoproliferative Syndromes, AutoimmuneC1328840
- Syndrome, Autoimmune LymphoproliferativeC1328840
- Syndrome, Canale SmithC1328840
- Syndrome, Canale-SmithC1328840
- Syndromes, Autoimmune LymphoproliferativeC1328840
- Syndromes, Canale-SmithC1328840
- autoimmune lymphoproliferative syndromeC1328840
Clinical Terms
- Syndromes, Autoimmune Lymphoproliferative
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
- Syndrome, Canale-Smith
- Canale-Smith syndrome
- Dianzani autoimmune lymphoproliferative disease
- Autoimmune lymphoproliferative syndrome type 4
- Canale Smith Syndrome
- DALD - Dianzani autoimmune lymphoproliferative disease
- Lymphoproliferative Syndrome, Autoimmune
- RALD - RAS-associated autoimmune leucoproliferative disease
- autoimmune lymphoproliferative syndrome
- STAT3-related early-onset multisystem autoimmune disease
- ALPS - autoimmune lymphoproliferative syndrome
- AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT
- Autoimmune lymphoproliferative syndrome (disorder)
- Syndrome, Autoimmune Lymphoproliferative
- RAS-associated autoimmune leukoproliferative disease
- Autoimmune lymphoproliferative syndrome with recurrent viral infection
- Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease
- ALPS
- CTLA-4 haploinsufficiency with autoimmune infiltration disease
- Syndromes, Canale-Smith
- Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency
- RAS-associated autoimmune leucoproliferative disease
- Canale-Smith Syndromes
- Autoimmune Lymphoproliferative Syndromes
- RALD - RAS-associated autoimmune leukoproliferative disease
- Syndrome, Canale Smith
- Caspase 8 deficiency syndrome
- Autoimmune lymphoproliferative syndrome type IV
- ALPS (autoimmune lymphoproliferative syndrome)
- Lymphoproliferative Syndromes, Autoimmune
Frequently Asked Questions
What is the ICD-10 code for autoimmune lymphoproliferative syndrome [alps]?
The ICD-10-CM code for autoimmune lymphoproliferative syndrome [alps] is D89.82. The full clinical description is "Autoimmune lymphoproliferative syndrome [ALPS]". D89.82 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D89.82 mean?
ICD-10-CM code D89.82 represents “Autoimmune lymphoproliferative syndrome [ALPS]”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D89.82 a billable code?
Yes, D89.82 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D89.82 in?
D89.82 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D89.82?
D89.82 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 2 more.
What SNOMED CT codes does D89.82 map to?
D89.82 maps to 6 SNOMED CT concepts: 702444009, 1197361002, 723508002, 722290008, 721093000, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D89.82?
D89.82 is linked to 1 UMLS Concept Unique Identifier: C1328840. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D89.82 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like autoimmune lymphoproliferative syndrome [alps] 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 D89.82?
There is no direct ICD-11 mapping available for D89.82 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.