D69.1

Qualitative platelet defects

Non-billable headerHCC V28 112

D69.1 is a non-billable header code. Use one of the more specific codes below.

Excludes1

Not coded here — never report together with this code.

hemolytic-uremic syndrome (D59.3-)
benign hypergammaglobulinemic purpura (D89.0) (from D69)
cryoglobulinemic purpura (D89.1) (from D69)
essential (hemorrhagic) thrombocythemia (D47.3) (from D69)
hemorrhagic thrombocythemia (D47.3) (from D69)
purpura fulminans (D65) (from D69)
thrombotic thrombocytopenic purpura (M31.19) (from D69)
Waldenström hypergammaglobulinemic purpura (D89.0) (from D69)

Not included here — may be reported together when both conditions exist.

von Willebrand disease (D68.0-)
autoimmune disease (systemic) NOS (M35.9) (from D69)
certain conditions originating in the perinatal period (P00-P96) (from D69)
complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D69)
congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D69)
endocrine, nutritional and metabolic diseases (E00-E88) (from D69)
human immunodeficiency virus [HIV] disease (B20) (from D69)
injury, poisoning and certain other consequences of external causes (S00-T88) (from D69)
neoplasms (C00-D49) (from D69)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D69)