Hereditary coagulation factor VIII deficiency (classic hemophilia A): Difference between revisions

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== Additional Info ==
== Additional Info ==


Hemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.[3][2] This results in people bleeding longer after an injury, easy bruising, and an increased risk of bleeding inside joints or the brain.  There are two main types of haemophilia: haemophilia A, which occurs due to not enough clotting factor VIII, and haemophilia B, which occurs due to not enough clotting factor IX.
Hemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding. This results in people bleeding longer after an injury, easy bruising, and an increased risk of bleeding inside joints or the brain.  There are two main types of haemophilia: haemophilia A, which occurs due to not enough clotting factor VIII, and haemophilia B, which occurs due to not enough clotting factor IX.


https://en.wikipedia.org/wiki/Haemophilia
https://en.wikipedia.org/wiki/Haemophilia
== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
*[[Hereditary coagulation factor IX deficiency (Christmas disease, hemophilia B)]]
*[[Hereditary coagulation factor IX deficiency (Christmas disease, hemophilia B)]]
*[[Hereditary deficiency of clotting factor, NOS]]


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==

Revision as of 17:42, 2018 April 2

ICD10 Diagnosis
Dx: Hereditary coagulation factor VIII deficiency (classic hemophilia A)
ICD10 code: D66
Pre-ICD10 counterpart: Hemophilia
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • D66
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
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Additional Info

Hemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding. This results in people bleeding longer after an injury, easy bruising, and an increased risk of bleeding inside joints or the brain. There are two main types of haemophilia: haemophilia A, which occurs due to not enough clotting factor VIII, and haemophilia B, which occurs due to not enough clotting factor IX.

https://en.wikipedia.org/wiki/Haemophilia

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Related Articles

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