Alphabetic Index · main term
Parahemophilia
At the main termsee also Defect, coagulation
Parahemophilia is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists D68.2 for this term: Hereditary deficiency of other clotting factors. It is a billable code. Also see Defect, coagulation. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Hereditary deficiency of other clotting factors
Where the Index sends you
see also Defect, defective, coagulation (factor)
Coagulation defect, unspecified
First-level subterms 9
Other Index terms that lead to D68.2
Different words, same code. 50 entries
- Absence (of) (organ or part) (complete or partial), fibrinogen (congenital)
- Afibrinogenemia, congenital
- Defect, defective, coagulation (factor), hereditary NEC
- Defect, defective, fibrin polymerization
- Defect, defective, Hageman (factor)
- Deficiency, deficient, AC globulin (congenital) (hereditary)
- Deficiency, deficient, accelerator globulin (Ac G) (blood)
- Deficiency, deficient, activating factor (blood)
- Deficiency, deficient, autoprothrombin, C
- Deficiency, deficient, autoprothrombin, I
- Deficiency, deficient, clotting factor NEC (hereditary)
- Deficiency, deficient, coagulation NOS, clotting factor NEC
Show 38 more
- Deficiency, deficient, contact factor
- Deficiency, deficient, factor, Hageman
- Deficiency, deficient, factor, I (congenital) (hereditary)
- Deficiency, deficient, factor, II (congenital) (hereditary)
- Deficiency, deficient, factor, V (congenital) (hereditary)
- Deficiency, deficient, factor, VII (congenital) (hereditary)
- Deficiency, deficient, factor, X (congenital) (hereditary)
- Deficiency, deficient, factor, XII (congenital) (hereditary)
- Deficiency, deficient, factor, XIII (congenital) (hereditary)
- Deficiency, deficient, fibrin-stabilizing factor (congenital) (hereditary)
- Deficiency, deficient, fibrinase
- Deficiency, deficient, fibrinogen (congenital) (hereditary)
- Deficiency, deficient, glass factor
- Deficiency, deficient, Hageman factor
- Deficiency, deficient, labile factor (congenital) (hereditary)
- Deficiency, deficient, Laki-Lorand factor
- Deficiency, deficient, proaccelerin (congenital) (hereditary)
- Deficiency, deficient, proconvertin factor (congenital) (hereditary)
- Deficiency, deficient, prothrombin (congenital) (heredItary)
- Deficiency, deficient, Prower factor
- Deficiency, deficient, SPCA (factor VII)
- Deficiency, deficient, stable factor (congenital) (hereditary)
- Deficiency, deficient, Stuart-Prower (factor X)
- Deficiency, deficient, thrombokinase
- Disease, diseased, Hageman (congenital factor XII deficiency)
- Disease, diseased, Stuart's (congenital factor X deficiency)
- Disease, diseased, Stuart-Prower (congenital factor X deficiency)
- Dysfibrinogenemia (congenital)
- Fibrinogenopenia, congenital
- Fibrinopenia (hereditary)
- Hageman's factor defect, deficiency or disease
- Hypofibrinogenemia, congenital (hereditary)
- Hypoproconvertinemia, congenital (hereditary)
- Hypoprothrombinemia (congenital) (hereditary) (idiopathic)
- Owren's disease or syndrome (parahemophilia)
- Stuart deficiency disease (factor X)
- Stuart-Prower factor deficiency (factor X)
- Syndrome, Owren's