Code
Hierarchy
-
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
Inclusion Terms
D69.42
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Congenital thrombocytopenia
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Hereditary thrombocytopenia
Code First
D69.42
-
congential or hereditary disorder, such as:
-
thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
- Q87.2 Congenital malformation syndromes predominantly involving limbs
Excludes 1
-
benign hypergammaglobulinemic purpura (D89.0)
- D89.0 Polyclonal hypergammaglobulinemia
-
cryoglobulinemic purpura (D89.1)
- D89.1 Cryoglobulinemia
- D47.3 Essential (hemorrhagic) thrombocythemia
-
hemorrhagic thrombocythemia (D47.3)
- D47.3 Essential (hemorrhagic) thrombocythemia
-
purpura fulminans (D65)
- D65 Disseminated intravascular coagulation [defibrination syndrome]
-
thrombotic thrombocytopenic purpura (M31.19)
- M31.19 Other thrombotic microangiopathy
-
Waldenström hypergammaglobulinemic purpura (D89.0)
- D89.0 Polyclonal hypergammaglobulinemia
Excludes 2
-
autoimmune disease (systemic) NOS (M35.9)
- M35.9 Systemic involvement of connective tissue, unspecified
- P00-P96 Certain conditions originating in the perinatal period (P00-P96)
-
complications of pregnancy, childbirth and the puerperium (O00-O9A)
- O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
- Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
-
endocrine, nutritional and metabolic diseases (E00-E88)
- B20 Human immunodeficiency virus [HIV] disease
- S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
- C00-D49 Neoplasms (C00-D49)
-
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)