Alphabetic Index · main term
Bruton's X-linked agammaglobulinemia
Bruton's X-linked agammaglobulinemia is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists D80.0 for this term: Hereditary hypogammaglobulinemia. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Hereditary hypogammaglobulinemia
Other Index terms that lead to D80.0
Different words, same code. 13 entries
- Absence (of) (organ or part) (complete or partial), gamma globulin in blood, hereditary
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), autosomal recessive (Swiss type)
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), Bruton's X-linked
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), congenital sex-linked
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), hereditary
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), Swiss type (autosomal recessive)
- Agammaglobulinemia (acquired (secondary)) (nonfamilial), X-linked (with growth hormone deficiency) (Bruton)
- Deficiency, deficient, gammaglobulin in blood, hereditary
- Hypogammaglobulinemia, hereditary
- Immunodeficiency, autosomal recessive, Swiss type
- Syndrome, antibody deficiency, agammaglobulinemic, hereditary
- Syndrome, antibody deficiency, congenital