D80.0 – Hereditary hypogammaglobulinemia
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Applicable To
Autosomal recessive agammaglobulinemia (Swiss type)
X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
GEM Conversion to ICD-9 CM
Fs: 00000
–
Congenital hypogammaglobulinemia
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Absence
(of) (organ or part) (complete or partial)
Agammaglobulinemia
(acquired (secondary)) (nonfamilial)
D80.1
autosomal recessive
(Swiss type)
D80.0
Swiss type
(autosomal recessive)
D80.0
Deficiency, deficient
Syndrome
See also Disease
Sibling Codes
Parent Sibling Codes
View in Tabular
| Code | Title |
|---|---|
| D50-D89 | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) |
| D80-D89 | Certain disorders involving the immune mechanism (D80-D89) |
| D80 | Immunodeficiency with predominantly antibody defects |
| D80.0 |
Hereditary hypogammaglobulinemia
Applicable to
Autosomal recessive agammaglobulinemia (Swiss type)
X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
|