ICD 10 CM Codes

D69.42 Congenital and hereditary thrombocytopenia purpura
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D69.42 converts approximately to:ICD-9-CM
2015 ICD-9-CM 287.33 Congenital and hereditary thrombocytopenic purpura
ICD-10-CM D69.42is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
813 COAGULATION DISORDERS
Alternate Description
Congenital thrombocytopenia
Hereditary thrombocytopenia
Code first
congential or hereditary disorder, such as:
thrombocytopenia with absent radius (TAR syndrome) (Q87.2)
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D69.42.'
Purpura; thrombocytopenic; congenital
Purpura; thrombocytopenic; hereditary
Thrombocytopenia, thrombocytopenic; congenital
Thrombocytopenia, thrombocytopenic; hereditary