Collagen-vascular disease, NOS: Difference between revisions

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{{ICD10 transition status

| OldDxArticle =Other CollVasc Diseases| CurrentStatus = ~~manually added for testing~~

| OldDxArticle =Other CollVasc Diseases

| CurrentStatus = reconciled

| InitialEditorAssigned = Marla Penner

~~| MinimumCombinedCodes =~~

}}

{{ICD10 dx

| MinimumCombinedCodes =

| ICD10 Code=M35.9

| BugRequired=

}}

{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Hereditary/congenital}}{{ICD10 category|Rheumatic disease}}{{ICD10 category|Vasculitis}}

== Additional Info ==

~~{sc:PAN, Churg-Strauss, Kawasaki, Goodpastures, TTP, Wegener~~'~~s, Takayasu~~'~~s, Giant cell arteritis, SLE~~, DM/~~PM, scleroderma, Overlap syndromes, Behcet's~~, ~~polymyalgia rheumatica}~~

Collagen vascular disease is sometimes also called connective tissue disease. Collagen vascular diseases can be heritable (inherited from one’s parents) or autoimmune (resulting from activity of the body’s immune system against itself).

'''Includes'''

*Ehlers Danlos syndrome, combine with [[Malformation/disorder NOS, congenital]]

* connective tissue disease

== Alternate ICD10s to consider coding instead ==

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

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

* [[Polyarteritis nodosa (PAN)]]

~~{sc:PAN,~~ Churg-Strauss, Kawasaki~~, Goodpastures,~~ TTP, Wegener's, Takayasu's, Giant cell arteritis, SLE, DM/~~PM, scleroderma, Overlap syndromes,~~ Behcet's~~, polymyalgia~~ rheumatica}

* [[Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis)]]

* [[Kawasaki disease (mucocutaneous lymph node syndrome)]]

* [[Goodpasture syndrome (hypersensitivity angiitis)]]

* [[Thrombotic thrombocytopenic purpura (TTP)]]

* [[Wegener's Granulomatosis / Granulomatosis with polyangiitis]]

* [[Takayasu's arteritis (aortic arch syndrome)]]

* [[Giant cell arteritis/temporal arteritis]]

* [[Systemic lupus erythematosis (SLE, lupus)]]

* [[Dermatomyositis/polymyositis]]

* [[Scleroderma or CREST syndrome (systemic sclerosis)]]

* [[Collagen-vascular overlap syndrome]]

* [[Behcet's disease]]

* [[Polymyalgia rheumatica]]

* [[:Category:Rheumatic disease]]

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

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

== Related CCI Codes ==

== Related Articles ==

@@ Line 1: / Line 1: @@
 {{ICD10 transition status
-| OldDxArticle =Other CollVasc Diseases| CurrentStatus = manually added for testing
+| OldDxArticle =Other CollVasc Diseases
+| CurrentStatus = reconciled
 | InitialEditorAssigned = Marla Penner
-| MinimumCombinedCodes =
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=M35.9
 | BugRequired=
 }}
+{{ICD10 category|Musculoskeletal/soft tissue}}{{ICD10 category| Heme/immunology}}{{ICD10 category|Hereditary/congenital}}{{ICD10 category|Rheumatic disease}}{{ICD10 category|Vasculitis}}
 == Additional Info ==
-{sc:PAN, Churg-Strauss, Kawasaki, Goodpastures, TTP, Wegener's, Takayasu's, Giant cell arteritis, SLE, DM/PM, scleroderma, Overlap syndromes, Behcet's, polymyalgia rheumatica}
+Collagen vascular disease is sometimes also called connective tissue disease. Collagen vascular diseases can be heritable (inherited from one’s parents) or autoimmune (resulting from activity of the body’s immune system against itself).
+'''Includes'''
+*Ehlers Danlos syndrome, combine with [[Malformation/disorder NOS, congenital]]
+* connective tissue disease
-== Alternate ICD10s to consider coding instead ==
+== Alternate ICD10s to consider coding instead or in addition ==
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+* [[Polyarteritis nodosa (PAN)]]
-{sc:PAN, Churg-Strauss, Kawasaki, Goodpastures, TTP, Wegener's, Takayasu's, Giant cell arteritis, SLE, DM/PM, scleroderma, Overlap syndromes, Behcet's, polymyalgia rheumatica}
+* [[Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis (EGPA), allergic granulomatous angiitis)]]
+* [[Kawasaki disease (mucocutaneous lymph node syndrome)]]
+* [[Goodpasture syndrome (hypersensitivity angiitis)]]
+* [[Thrombotic thrombocytopenic purpura (TTP)]]
+* [[Wegener's Granulomatosis / Granulomatosis with polyangiitis]]
+* [[Takayasu's arteritis (aortic arch syndrome)]]
+* [[Giant cell arteritis/temporal arteritis]]
+* [[Systemic lupus erythematosis (SLE, lupus)]]
+* [[Dermatomyositis/polymyositis]]
+* [[Scleroderma or CREST syndrome (systemic sclerosis)]]
+* [[Collagen-vascular overlap syndrome]]
+* [[Behcet's disease]]
+* [[Polymyalgia rheumatica]]
+* [[:Category:Rheumatic disease]]
 == Candidate [[Combined ICD10 codes]] ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
+== Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}