D69.1 – Qualitative platelet defects
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Type 1 Excludes
von Willebrand's disease (D68.0)
Applicable To
Bernard-Soulier [giant platelet] syndrome
Glanzmann's disease
Grey platelet syndrome
Thromboasthenia (hemorrhagic) (hereditary)
Thrombocytopathy
GEM Conversion to ICD-9 CM
Fs: 00000
–
Qualitative platelet defects
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Deficiency, deficient
Disease, diseased
See also Syndrome
Bernard-Soulier
(thrombopathy)
D69.1
Glanzmann's
(hereditary hemorrhagic thrombasthenia)
D69.1
Disorder
(of)
See also Disease
Dysfunction
Glanzmann disease or thrombasthenia
(-Naegeli)
D69.1
Syndrome
See also Disease
giant platelet
(Bernard-Soulier)
D69.1
gray or grey
(newborn)
P93.0
Thrombasthenia
(Glanzmann) (hemorrhagic) (hereditary)
D69.1
Thromboasthenia
(Glanzmann) (hemorrhagic) (hereditary)
D69.1
Thrombocytasthenia
(Glanzmann)
D69.1
Thrombocytopathy
(dystrophic) (granulopenic)
D69.1
Thrombopathy
(Bernard-Soulier)
D69.1
Sibling Codes
Parent Sibling Codes
View in Tabular
Code | Title |
---|---|
D50-D89 | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) |
D65-D69 | Coagulation defects, purpura and other hemorrhagic conditions (D65-D69) |
D69 | Purpura and other hemorrhagic conditions |
D69.1 |
Qualitative platelet defects
Type 1 Excludes
von Willebrand's disease (D68.0)
Applicable to
Bernard-Soulier [giant platelet] syndrome
Glanzmann's disease
Grey platelet syndrome
Thromboasthenia (hemorrhagic) (hereditary)
Thrombocytopathy
|