D81.39
Other adenosine deaminase deficiency
HCC risk adjustment mapping
CMS-HCC V28
Common Variable and Combined Immunodeficiencies
CMS-HCC ESRD V24
Disorders of Immunity
RxHCC V08
Immune Disorders
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Adenosine deaminase [ADA] deficiency type 1, NOS Adenosine deaminase [ADA] deficiency type 1, without SCID Adenosine deaminase [ADA] deficiency type 1, without severe combined immunodeficiency Partial ADA deficiency (type 1) Partial adenosine deaminase deficiency (type 1)
autosomal recessive agammaglobulinemia (Swiss type) (D80.0)
autoimmune disease (systemic) NOS (M35.9) certain conditions originating in the perinatal period (P00-P96) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) human immunodeficiency virus [HIV] disease (B20) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Official Guidelines for D81.39
FY 2026 ›Find D81.39 in the alphabetic index
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