ICD-10-CM Code D80.0
Hereditary hypogammaglobulinemia
BILLABLE
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ICD-10 from 2011 - 2016
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.D80.0 is a billable ICD code used to specify a diagnosis of hereditary hypogammaglobulinemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
Coding Notes for D80.0 Info for medical coders on how to properly use this ICD-10 code
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Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive. - Autosomal recessive agammaglobulinemia (Swiss type)
- X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
MS-DRG Mapping
- DRG Group #814-816 - Reticuloendothelial and immunity disorders with MCC.
- DRG Group #814-816 - Reticuloendothelial and immunity disorders with CC.
- DRG Group #814-816 - Reticuloendothelial and immunity disorders without CC or MCC.
Related Concepts SNOMET-CT
- Autosomal recessive hyperimmunoglobulin M syndrome (finding)
ICD-10-CM Alphabetical Index References for 'D80.0 - Hereditary hypogammaglobulinemia'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D80.0. Click on any term below to browse the alphabetical index.
Bruton's X-linked agammaglobulinemia (D80.0)
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
Congenital hypogammaglobulinemia
(exact match)
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 279.04 was previously used, D80.0 is the appropriate modern ICD10 code.
Parent Code: D80 - Immunodeficiency with predominantly antibody defects