Hereditary coagulation factor VIII deficiency (classic hemophilia A): Difference between revisions
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{{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}} | {{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}}{{ICD10 category|Hemophilia}} | ||
== 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. 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 == | ||
{{DA | I made the category Hemophila since [[Disease of blood or blood-forming organ, NOS]] had it as an SC and I needed to be able to link it. Is the list now grouped complete? If not, pls add <nowiki>{{ICD10 category|Hemophilia}}</nowiki> to other pages as appropriate. }} | |||
{{ListICD10Category | categoryName = Hemophilia}} | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
Revision as of 18:01, 2019 January 3
| 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.
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
|
I made the category Hemophila since Disease of blood or blood-forming organ, NOS had it as an SC and I needed to be able to link it. Is the list now grouped complete? If not, pls add {{ICD10 category|Hemophilia}} to other pages as appropriate. |
| Hemophilia codes: |
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
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