Creutzfeldt-Jakob disease: Difference between revisions

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{{ICD10 transition status

| OldDxArticle =~~Other Problems~~| CurrentStatus = ~~manually added for testing~~

| OldDxArticle = CJD-Creutzfeldt-Jakob Disease

| CurrentStatus = reconciled

| InitialEditorAssigned = Allyson Alcudia

~~| MinimumCombinedCodes =~~

}}

{{ICD10 dx

| MinimumCombinedCodes =

| ICD10 Code=A81.0

| BugRequired=

}}

== Additional Info ==

* CJD develops in three ways:

** Sporadically. Most people with Creutzfeldt-Jakob disease develop the disease for no apparent reason. This type, called spontaneous CJD or sporadic CJD, accounts for most cases.

** By inheritance. Fewer than 15% of people with CJD have a family history. They may test positive for genetic changes associated with the disease. This type is referred to as familial CJD.

** By contamination. A small number of people have developed CJD as a result of medical procedures (contaminated instruments or from injections of growth hormone.

** A small number of people have developed variant CJD from eating contaminated beef. Variant CJD is linked to eating beef from cattle infected with mad cow disease. Mad cow disease is known as bovine spongiform encephalopathy (BSE).

== Alternate ICD10s to consider coding instead or in addition ==

== ~~Alternate ICD10s to consider coding instead~~ ==

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

~~(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)~~

== Related CCI Codes ==

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

~~(put links to likely candidates coded with this one, eg. a cause for a trauma.)~~

== Related Articles ==

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 {{ICD10 transition status
-| OldDxArticle =Other Problems| CurrentStatus = manually added for testing
+| OldDxArticle = CJD-Creutzfeldt-Jakob Disease
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Allyson Alcudia
-| MinimumCombinedCodes =
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=A81.0
 | BugRequired=
 }}
+{{ICD10 category|Infectious disease}}{{ICD10 category|Infection with implied pathogen}}{{ICD10 category|Neuro}}
 == Additional Info ==
+* CJD develops in three ways:
+** Sporadically. Most people with Creutzfeldt-Jakob disease develop the disease for no apparent reason. This type, called spontaneous CJD or sporadic CJD, accounts for most cases.
+** By inheritance. Fewer than 15% of people with CJD have a family history. They may test positive for genetic changes associated with the disease. This type is referred to as familial CJD.
+** By contamination. A small number of people have developed CJD as a result of medical procedures (contaminated instruments or from injections of growth hormone.
+** A small number of people have developed variant CJD from eating contaminated beef. Variant CJD is linked to eating beef from cattle infected with mad cow disease. Mad cow disease is known as bovine spongiform encephalopathy (BSE).
+== Alternate ICD10s to consider coding instead or in addition ==
-== Alternate ICD10s to consider coding instead ==
+== Candidate [[Combined ICD10 codes]] ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+{{ICD10 Guideline Infection}}
+== Related CCI Codes ==
-== Candidate [[Combined ICD10 codes]] ==
+{{Data Integrity Check List}}
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}