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) 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)
- transplant failure and rejection (T86.-)
Also Known As / Clinical Terms
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
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.
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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.