ICD 10 CM Codes

D80.0 Hereditary hypogammaglobulinemia
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D80.0 converts approximately to:ICD-9-CM
2015 ICD-9-CM 279.04 Congenital hypogammaglobulinemia
ICD-10-CM D80.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
814 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC
815 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC
816 RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC
Alternate Description
Autosomal recessive agammaglobulinemia (Swiss type)
X-linked agammaglobulinemia [Bruton] (with growth hormone deficiency)
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D80.0.'
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)
Bruton's X-linked agammaglobulinemia
Deficiency, deficient; gammaglobulin in blood; hereditary
Hypogammaglobulinemia; hereditary
Immunodeficiency; autosomal recessive, Swiss type
Syndrome; antibody deficiency; agammaglobulinemic; hereditary
Syndrome; antibody deficiency; congenital
Syndrome; antibody deficiency; hypogammaglobulinemic; hereditary