Difference between revisions of "Template:Lymphoid and complement immunodeficiency"
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imported>Tom (LT) m (per Template_talk:Medicine_navs#Background_colours, remove unnecessary and confusing background colours using AWB) |
imported>NSH002 (tidy up) |
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{{Navbox | {{Navbox | ||
| − | | name | + | | name = Lymphoid and complement immunodeficiency |
| − | | title = [[Immune disorder]]s: [[Lymphatic system|Lymphoid]] and [[Complement system|complement]] [[immunodeficiency]] ([[ICD-10 Chapter II: Neoplasms; Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism#(D80–D89) Certain disorders involving the immune mechanism|D80–D85]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Disorders involving the immune mechanism|279.0–4]]) | + | | title = [[Immune disorder]]s: [[Lymphatic system|Lymphoid]] and [[Complement system|complement]] [[immunodeficiency]] ([[ICD-10 Chapter II: Neoplasms; Chapter III: Diseases of the blood and blood-forming organs, and certain disorders involving the immune mechanism#(D80–D89) Certain disorders involving the immune mechanism|D80–D85]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Disorders involving the immune mechanism|279.0–4]]) |
| − | |listclass = hlist | + | | state = {{{state|}}} |
| + | | listclass = hlist | ||
| + | | group1 = [[Primary immunodeficiency|Primary]] | ||
| + | | list1 = {{Navbox|child | ||
| + | | group1 = [[Antibody]]/[[Humoral immune deficiency|humoral]] ([[B cell|B]]) | ||
| + | | list1 = {{Navbox|child | ||
| − | + | | group1 = [[Hypogammaglobulinemia]] | |
| − | + | | list1 = | |
| − | |||
| − | |||
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| − | |||
| − | |||
| − | | group1 = [[Hypogammaglobulinemia]] | ||
| − | | list1 | ||
* [[X-linked agammaglobulinemia]] | * [[X-linked agammaglobulinemia]] | ||
* [[Transient hypogammaglobulinemia of infancy]] | * [[Transient hypogammaglobulinemia of infancy]] | ||
| − | | group2 = [[Dysgammaglobulinemia]] | + | | group2 = [[Dysgammaglobulinemia]] |
| − | | list2 | + | | list2 = |
* [[Selective immunoglobulin A deficiency|IgA deficiency]] | * [[Selective immunoglobulin A deficiency|IgA deficiency]] | ||
* [[Selective deficiency of immunoglobulin G|IgG deficiency]] | * [[Selective deficiency of immunoglobulin G|IgG deficiency]] | ||
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* [[Hyperimmunoglobulin E syndrome|Hyper-IgE syndrome]] | * [[Hyperimmunoglobulin E syndrome|Hyper-IgE syndrome]] | ||
| − | |group3 | + | | group3 = Other |
| − | |list3 | + | | list3 = |
* [[Common variable immunodeficiency]] | * [[Common variable immunodeficiency]] | ||
* [[ICF syndrome]] | * [[ICF syndrome]] | ||
| − | }} | + | }} |
| − | + | | group2 = [[T cell deficiency]] ([[T cell|T]]) | |
| − | + | | list2 = | |
* ''[[thymic hypoplasia]]:'' ''hypoparathyroid'' ([[DiGeorge syndrome|Di George's syndrome]]) | * ''[[thymic hypoplasia]]:'' ''hypoparathyroid'' ([[DiGeorge syndrome|Di George's syndrome]]) | ||
* ''euparathyroid'' ([[Nezelof syndrome]] | * ''euparathyroid'' ([[Nezelof syndrome]] | ||
| − | * [[Ataxia telangiectasia]]) | + | * [[Ataxia telangiectasia]]) |
| − | + | ''peripheral:'' [[Purine nucleoside phosphorylase deficiency]] | |
| − | * [[Hyper IgM syndrome]] ([[Hyper-IgM syndrome type 1|1]]) | + | * [[Hyper IgM syndrome]] ([[Hyper-IgM syndrome type 1|1]]) |
| − | + | | group3 = [[Severe combined immunodeficiency|Severe]] [[Combined immunodeficiencies|combined]] (B+T) | |
| − | + | | list3 = | |
* ''x-linked:'' [[X-linked severe combined immunodeficiency|X-SCID]]<br />''autosomal:'' [[Adenosine deaminase deficiency]] | * ''x-linked:'' [[X-linked severe combined immunodeficiency|X-SCID]]<br />''autosomal:'' [[Adenosine deaminase deficiency]] | ||
* [[Omenn syndrome]] | * [[Omenn syndrome]] | ||
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* [[Bare lymphocyte syndrome]] | * [[Bare lymphocyte syndrome]] | ||
| − | + | }} | |
| − | + | | group2 = [[Immunodeficiency#acquired|Acquired]] | |
| − | + | | list2 = | |
* [[AIDS]] | * [[AIDS]] | ||
| − | | | + | | group3 = [[Leukopenia]]:<br />[[Lymphocytopenia]] |
| − | | | + | | list3 = |
* [[Idiopathic CD4+ lymphocytopenia]] | * [[Idiopathic CD4+ lymphocytopenia]] | ||
| − | + | | group4 = [[Complement deficiency]] | |
| − | + | | list4 = | |
* ''[[C1-inhibitor]]'' ([[Angioedema]]/[[Hereditary angioedema]]) | * ''[[C1-inhibitor]]'' ([[Angioedema]]/[[Hereditary angioedema]]) | ||
* [[Complement 2 deficiency]]/[[Complement 4 deficiency]] | * [[Complement 2 deficiency]]/[[Complement 4 deficiency]] | ||
| Line 74: | Line 71: | ||
* [[Complement receptor deficiency]] | * [[Complement receptor deficiency]] | ||
| − | | | + | | belowstyle = background: transparent; padding: 0px; |
| − | | | + | | below = {{Lymph cell navs}} |
}}<noinclude> | }}<noinclude> | ||
| + | {{collapsible option}} | ||
[[Category:Disease and disorder templates]] | [[Category:Disease and disorder templates]] | ||
| − | |||
| − | |||
| − | |||
[[Category:Immunology templates]] | [[Category:Immunology templates]] | ||
</noinclude> | </noinclude> | ||
Revision as of 12:58, 6 April 2015
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state= parameter may be used:
|state=collapsed:{{Lymphoid and complement immunodeficiency|state=collapsed}}to show the template collapsed, i.e., hidden apart from its title bar|state=expanded:{{Lymphoid and complement immunodeficiency|state=expanded}}to show the template expanded, i.e., fully visible|state=autocollapse:{{Lymphoid and complement immunodeficiency|state=autocollapse}}
If the |state= parameter in the template on this page is not set, the template's initial visibility is taken from the |default= parameter in the Collapsible option template. For the template on this page, that currently evaluates to autocollapse.