ICD 10 CM Codes

D68.1 Hereditary factor XI deficiency
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D68.1 converts approximately to:ICD-9-CM
2015 ICD-9-CM 286.2 Congenital factor XI deficiency
ICD-10-CM D68.1is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
813 COAGULATION DISORDERS
Alternate Description
Hemophilia C
Plasma thromboplastin antecedent [PTA] deficiency
Rosenthal's disease
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D68.1.'
Deficiency, deficient; anti-hemophilic; factor (A); C
Deficiency, deficient; factor; XI (congenital) (hereditary)
Deficiency, deficient; plasma thromboplastin; antecedent (PTA)
Deficiency, deficient; PTA (plasma thromboplastin antecedent)
Disease, diseased; Rosenthal's (factor XI deficiency)
Hemophilia (classical) (familial) (hereditary); C
Rosenthal's disease or syndrome