ICD-10-CM Code D68.1
Hereditary factor XI deficiency
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
D68.1 is a billable ICD code used to specify a diagnosis of hereditary factor XI deficiency. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code D681 is used to code Haemophilia C
Haemophilia C (also known as plasma thromboplastin antecedent (PTA) deficiency or Rosenthal syndrome) is a mild form of haemophilia affecting both sexes. However, it predominantly occurs in Jews of Ashkenazi descent. It is the fourth most common coagulation disorder after von Willebrand's disease and haemophilia A and B. In the USA it is thought to affect 1 in 100,000 of the adult population, making it 10% as common as haemophilia A.
|ICD 9 Code:||286.2|
Coding Notes for D68.1 Info for medical coders on how to properly use this ICD-10 code
Inclusion TermsInclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
- Hemophilia C
- Plasma thromboplastin antecedent [PTA] deficiency
- Rosenthal's disease
- DRG Group #813 - Coagulation disorders.
ICD-10-CM Alphabetical Index References for 'D68.1 - Hereditary factor XI deficiency'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D68.1. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 286.2 was previously used, D68.1 is the appropriate modern ICD10 code.