Diagnoses of immunodeficiency with predominantly antibody defects
- Level
- Class
- Parent
- 85320000
- Below
- 8
- Links · KBLI
- 9
Definition
UNSPSC 85323000This classification denotes the group of activities that yields a diagnosis of Immunodeficiency With Predominantly Antibody Defects. Immunodeficiency With Predominantly Antibody Defects is listed In The World Health Organization's International Statistical Classification of Diseases and Related Health Problems or Icd-10 as a Three Digit Category under code A00. Icd-10 Also Has The Following Immunodeficiency With Predominantly Antibody Defects Children in its Four-Character Category: D80.0 or Hereditary Hypogammaglobulinaemia; D80.1 or Nonfamilial Hypogammaglobulinaemia; D80.2 or Selective Deficiency of Immunoglobulin A or Iga; D80.3 or Selective Deficiency of Immunoglobulin G or Igg Subclasses; D80.4 or Selective Deficiency of Immunoglobulin M or Igm; D80.5 or Immunodeficiency With Increased Immunoglobulin M or Igm; D80.6 or Antibody Deficiency With Near-Normal Immunoglobulins Or With Hyperimmunoglobulinaemia; D80.7 or Transient Hypogammaglobulinaemia of Infancy; D80.8 or Other Immunodeficiencies With Predominantly Antibody Defects; D80.9 or Immunodeficiency With Predominantly Antibody Defects, Unspecified. IMMUNODEFICIENCY WITH PREDOMINANTLY ANTIBODY DEFECTS is listed in the Centers For Medicare & Medicaid Services International Classification Of Diseases Clinical Modification (Tenth Revision) (Icd-10-CM) as a Three Digit Category under code D80. ICD-10-CM also has the following IMMUNODEFICIENCY WITH PREDOMINANTLY ANTIBODY DEFECTS CHILDREN in its Four-Character or Five-Character Categories: (HEREDITARY HYPOGAMMAGLOBULINEMIA D80.0), (NONFAMILIAL HYPOGAMMAGLOBULINEMIA D80.1), (SELECTIVE DEFICIENCY of IMMUNOGLOBULIN a [IGA] D80.2), (SELECTIVE DEFICIENCY of IMMUNOGLOBULIN G [IGG] SUBCLASSES D80.3), (SELECTIVE DEFICIENCY of IMMUNOGLOBULIN M [IGM] D80.4), (IMMUNODEFICIENCY WITH INCREASED IMMUNOGLOBULIN M [IGM] D80.5), (ANTIBODY DEFIC W NEAR-NORM IMMUNOGLOB or W HYPERIMMUNOGLOB D80.6), (TRANSIENT HYPOGAMMAGLOBULINEMIA of INFANCY D80.7), (OTHER IMMUNODEFICIENCIES WITH PREDOMINANTLY ANTIBODY DEFECTS D80.8), (IMMUNODEFICIENCY WITH PREDOMINANTLY ANTIBODY DEFECTS, UNSP D80.9).
Same parent
Under 85320000 · 22Activities that produce or sell this
KBLI · 9Inherited from family 85320000.
Warning
The links were generated with a large language model (Gemini 3.5 Flash), matching UNSPSC at the family level to KBLI at the kelompok level. Some of them maybe are wrong, so check any link you intend to rely on.