- D80.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM D80.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D80.0 – other international versions of ICD-10 D80.0 may differ.
ICD-10-CM D80.0 is grouped within Diagnostic Related Group(s):
- 814 Reticuloendothelial and immunity disorders with mcc
- 815 Reticuloendothelial and immunity disorders with cc
- 816 Reticuloendothelial and immunity disorders without cc/mcc
Applicable To
- Autosomal recessive agammaglobulinemia (Swiss type)
- X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to D80.0:
- hereditary > gamma globulin in blood D80.1
- autosomal recessive (Swiss type) > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- Bruton\’s X-linked > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- congenital sex-linked > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- hereditary > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- Swiss type (autosomal recessive) > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- X-linked (with growth hormone deficiency) (Bruton) > Agammaglobulinemia (acquired (secondary)) (nonfamilial) D80.1
- hereditary > gammaglobulin in blood D80.1
- hereditary > Hypogammaglobulinemia D80.1
- autosomal recessive, Swiss type > Immunodeficiency D84.9
- hereditary > agammaglobulinemic D80.1
- congenital > antibody deficiency D80.9
- hereditary > hypogammaglobulinemic D80.1