D81.31
BillableSevere combined immunodef due to adenosine deaminase defic
Severe combined immunodeficiency due to adenosine deaminase deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- ADA deficiency with SCID
- Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency
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
Related Codes(3)
Also Known As / Clinical Terms(60)
SNOMED CT
- Agammaglobulinaemia - Swiss type22406001
- SCID (severe combined immunodeficiency) due to absent lymphoid stem cells22406001
- Severe combined immunodeficiency due to absent lymphoid stem cells22406001
- Swiss type agammaglobulinemia22406001
- SCID (severe combined immunodeficiency) due to absent ADA (adenosine deaminase)36980009
- SCID (severe combined immunodeficiency) due to absent adenosine deaminase36980009
- Severe combined immunodeficiency due to absent adenosine deaminase36980009
UMLS
- ADA deficiency with SCIDC0392607
- ADA-SCIDC0392607
- Adenosine Deaminase DeficiencyC0392607
- Adenosine Deaminase Deficient Severe Combined ImmunodeficiencyC0392607
- Adenosine Deaminase Severe Combined Immune DeficiencyC0392607
- Adenosine Deaminase Severe Combined ImmunodeficiencyC0392607
- Adenosine deaminase [ADA] deficiency with severe combined immunodeficiencyC0392607
- Adenosine deaminase deficient severe combined immunodeficiencyC0392607
- Adenosine deaminase-deficient severe combined immunodeficiency diseaseC0392607
- Agammaglobulinaemia - Swiss typeC0392607
- Agammaglobulinemia, Swiss typeC0392607
- Bubble boy diseaseC0392607
- SCID (severe combined immunodeficiency) due to absent lymphoid stem cellsC0392607
- SCID DUE TO ADA DEFICIENCYC0392607
- SCID DUE TO ADA DEFICIENCY, EARLY-ONSETC0392607
- SCID Due to ADA DeficiencyC0392607
- SCID Due to ADA Deficiency, Early-OnsetC0392607
- SCID due to ADA deficiencyC0392607
- SCID1C0392607
- SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCYC0392607
- Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase DeficiencyC0392607
- Severe combined immunodef due to adenosine deaminase deficC0392607
- Severe combined immunodeficiency due to ADA deficiencyC0392607
- Severe combined immunodeficiency due to absent lymphoid stem cellsC0392607
- Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)C0392607
- Severe combined immunodeficiency due to adenosine deaminase deficiencyC0392607
- Severe combined immunodeficiency, alymphocytotic typeC0392607
- Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiencyC0392607
- Swiss type agammaglobulinemiaC0392607
Clinical Terms
- SCID DUE TO ADA DEFICIENCY, EARLY-ONSET
- Swiss type agammaglobulinemia
- Adenosine deaminase-deficient severe combined immunodeficiency disease
- SCID (severe combined immunodeficiency) due to absent ADA (adenosine deaminase)
- Adenosine Deaminase Deficient Severe Combined Immunodeficiency
- Severe combined immunodeficiency due to absent adenosine deaminase
- Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency
- Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)
- Adenosine Deaminase Deficiency
- Adenosine Deaminase Severe Combined Immunodeficiency
- Bubble boy disease
- Agammaglobulinemia, Swiss type
- SCID DUE TO ADA DEFICIENCY
- ADA-SCID
- SCID (severe combined immunodeficiency) due to absent lymphoid stem cells
- ADA deficiency with SCID
- SCID (severe combined immunodeficiency) due to absent adenosine deaminase
- Adenosine Deaminase Severe Combined Immune Deficiency
- Severe combined immunodeficiency due to ADA deficiency
- Severe combined immunodeficiency, alymphocytotic type
- Severe combined immunodeficiency due to absent lymphoid stem cells
- SCID1
- Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency
- Agammaglobulinaemia - Swiss type
Frequently Asked Questions
What is the ICD-10 code for severe combined immunodef due to adenosine deaminase defic?
The ICD-10-CM code for severe combined immunodef due to adenosine deaminase defic is D81.31. The full clinical description is "Severe combined immunodeficiency due to adenosine deaminase deficiency". D81.31 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D81.31 mean?
ICD-10-CM code D81.31 represents “Severe combined immunodeficiency due to adenosine deaminase deficiency”. 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 D81.31 a billable code?
Yes, D81.31 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D81.31 in?
D81.31 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D81.31?
D81.31 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 D81.31 map to?
D81.31 maps to 2 SNOMED CT concepts: 22406001, 36980009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D81.31?
D81.31 is linked to 1 UMLS Concept Unique Identifier: C0392607. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D81.31 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like severe combined immunodef due to adenosine deaminase defic 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 D81.31?
There is no direct ICD-11 mapping available for D81.31 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.