D81.2
BillableSevere combined immunodef w low or normal B-cell numbers
Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
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
- Severe combined immunodeficiency with low or normal B-cell numbers190998001
- SCIDX1 - severe combined immunodeficiency X-linked765145001
- T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency765145001
- T-B+ severe combined immunodeficiency due to gamma chain deficiency765145001
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to IL-7Ralpha deficiency1229940001
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency1229940001
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD45 deficiency1229941002
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency1229941002
- Autosomal recessive T- B+ severe combined immunodeficiency due to CD3D mutation1351209002
- Autosomal recessive T-B+ SCID (T-cell negative, B-cell positive severe combined immunodeficiency) due to CD3D mutation1351209002
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD3 delta subunit of T-cell receptor complex mutation1351209002
- Autosomal recessive T- B+ severe combined immunodeficiency due to CD3E mutation1351210007
- Autosomal recessive T-B+ SCID (T-cell negative, B-cell positive severe combined immunodeficiency) due to CD3E mutation1351210007
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD3 epsilon subunit of T-cell receptor complex mutation1351210007
- Autosomal recessive T- B+ severe combined immunodeficiency due to CD3Z mutation1351211006
- Autosomal recessive T-B+ SCID (T-cell negative, B-cell positive severe combined immunodeficiency) due to CD3-ZETA mutation1351211006
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to CD3-ZETA mutation1351211006
- Autosomal recessive T- B+ severe combined immunodeficiency due to SLP76 mutation1351212004
- Autosomal recessive T-B+ SCID (T-cell negative, B-cell positive severe combined immunodeficiency) due to SLP76 mutation1351212004
- Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to SLP76 mutation1351212004
UMLS
- Severe combined immunodef w low or normal B-cell numbersC0451694
- Severe combined immunodeficiency [SCID] with low or normal B-cell numbersC0451694
- Severe combined immunodeficiency with low or normal B-cell numbersC0451694
- Severe combined immunodeficiency with low or normal B-cell numbers (disorder)C0451694
Frequently Asked Questions
What is ICD-10 code D81.2?
ICD-10-CM code D81.2 represents "Severe combined immunodeficiency [SCID] with low or normal B-cell numbers". It is a billable/specific code that can be used on a claim.
Is D81.2 a billable code?
Yes, D81.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D81.2 in?
D81.2 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D81.2?
D81.2 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 D81.2 map to?
D81.2 maps to 8 SNOMED CT concepts: 1351209002, 1351210007, 1351211006, 1351212004, 1229941002, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D81.2?
D81.2 is linked to 1 UMLS Concept Unique Identifier: C0451694. 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.