Reserved for future guideline expansion
How to use this page
Everything the published sources say about one code, on one page.
- Read the Excludes1 block first — it is the one that stops you coding this at all alongside another code.
- Excludes2, Code first, Use additional and Includes follow. A note inherited from a parent category is labelled with the category it came from, so you can see why it applies.
- Official Guidelines sit below. "Guidelines naming this code" cite the code or a range containing it; "Chapter guidance" is the general guidance for its chapter and is the weaker signal.
- Guideline text is quoted verbatim with its section number and page, so you can check it against the published document.
- Risk-model chips show which published CMS models map this code.
What this page does not do
- Guidance is quoted, never paraphrased — a paraphrase of a coding rule is a different rule.
- Medication candidates, where shown, are matched by condition *name* and are offered as candidates for you to judge. They are not "the drugs for this code".
Exclusions13never code together
D68code
D50-D89chapter
Excludes2
- autoimmune disease (systemic) NOS (M35.9)M35.9
- certain conditions originating in the perinatal period (P00-P96)P00-P96
- complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
- endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
- human immunodeficiency virus [HIV] disease (B20)B20
- injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
- neoplasms (C00-D49)C00-D49
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94
Excludes1 — never code together. The excluded condition and this one are mutually exclusive.
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes2
D68.4code
Inclusion terms
- Deficiency of coagulation factor due to liver disease
- Deficiency of coagulation factor due to vitamin K deficiency
Official Guidelines1names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Index entries leading here6
- Deficiency, deficient
- AC globulin (congenital) (hereditary) D68.2
- acquired D68.4
- factor — see also Deficiency, coagulation
- fibrin-stabilizing factor (congenital) (hereditary) D68.2
- acquired D68.4
- labile factor (congenital) (hereditary) D68.2
- acquired D68.4
- proaccelerin (congenital) (hereditary) D68.2
- acquired D68.4
- proconvertin factor (congenital) (hereditary) D68.2
- acquired D68.4
- prothrombin (congenital) (heredItary) D68.2
- acquired D68.4
- stable factor (congenital) (hereditary) D68.2
- acquired D68.4
- coagulation NOS D68.9
- AC globulin (congenital) (hereditary) D68.2
- Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
- acquired D68.4
- Fibrinopenia (hereditary) D68.2
- acquired D68.4
- Defect, defective Q89.9
- Hemophilia (classical) (familial) (hereditary) D66
- Hyperprothrombinemia, causing coagulation factor deficiency D68.4
Alongside this code8same parent — D68
D68.0 Von Willebrand disease category D68.1 Hereditary factor XI deficiency D68.2 Hereditary deficiency of other clotting factors D68.3 Hemorrhagic disorder due to circulating anticoagulants category D68.5 Primary thrombophilia category D68.6 Other thrombophilia category D68.8 Other specified coagulation defects D68.9 Coagulation defect, unspecified
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.