Hemophilia: Difference between revisions

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{{DX tag | Hematology |  | Hemophilia | HEMOPHILIA | 22000 | Yes | 0 |  |  |  | }}
{{DX tag | Hematology |  | Hemophilia | HEMOPHILIA | 22000 | Yes | 0 |  |  |  | }}


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

Revision as of 08:45, 5 May 2017

Legacy Content

This page is about the pre-ICD10 diagnosis coding schema. See the ICD10 Diagnosis List, or the following for similar diagnoses in ICD10:Hereditary coagulation factor VIII deficiency (classic hemophilia A), Hereditary coagulation factor IX deficiency (Christmas disease, hemophilia B)

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edit dx infobox
Category/Organ
System:
Category: Hematology (old)

Type:

Medical Problem

Main Diagnosis: Hemophilia
Sub Diagnosis: HEMOPHILIA
Diagnosis Code: 22000
Comorbid Diagnosis: Yes
Charlson Comorbid coding (pre ICD10): 0
Program:
Status:


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.[

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