3B62.0 Inherited qualitative platelet defects

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

A disease caused by genetically inherited mutations leading to abnormalities in platelets. This disease is characterised by abnormal platelet formation or function. Confirmation is by identification of mutations by genetic testing.

code elsewhere

• Dense granule disease  (3B62.3)
• Alpha-delta dense granule deficiency  (3B62.4)

sections/codes in this section (3B62.0-3B62.0)

• Alpha-granule diseases  (3B62.00)
• Inherited giant platelet disorder  (3B62.01)
• Other specified inherited qualitative platelet defects  (3B62.0Y)
• Inherited qualitative platelet defects, unspecified  (3B62.0Z)

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