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Template:Lymphoid and complement immunodeficiency - Revision history
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http://christianpedia.com/index.php?title=Template:Lymphoid_and_complement_immunodeficiency&diff=15536&oldid=prev
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2024-05-24T18:11:09Z
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<p><b>New page</b></p><div>{{Navbox<br />
| name = Lymphoid and complement immunodeficiency<br />
| title = [[Lymphatic system|Lymphoid]] and [[Complement system|complement]] disorders causing [[immunodeficiency]]<br />
| state = {{{state|}}}<br />
| listclass = hlist<br />
<br />
| group1 = [[Primary immunodeficiency|Primary]]<br />
| list1 = {{Navbox|child<br />
<br />
| group1 = [[Antibody]]/[[Humoral immune deficiency|humoral]]<br/>([[B cell|B]])<br />
| list1 = {{Navbox|child<br />
<br />
| group1 = [[Hypogammaglobulinemia]]<br />
| list1 =<br />
* [[X-linked agammaglobulinemia]]<br />
* [[Transient hypogammaglobulinemia of infancy]]<br />
<br />
| group2 = [[Dysgammaglobulinemia]]<br />
| list2 =<br />
* [[Selective immunoglobulin A deficiency|IgA deficiency]]<br />
* [[IgG deficiency]]<br />
* [[Immunoglobulin M deficiency|IgM deficiency]]<br />
* [[Hyper IgM syndrome]] ([[Hyper-IgM syndrome type 1|1]]<br />
* [[Hyper-IgM syndrome type 2|2]]<br />
* [[Hyper-IgM syndrome type 3|3]]<br />
* [[Hyper-IgM syndrome type 4|4]]<br />
* [[Hyper-IgM syndrome type 5|5]])<br />
* [[Wiskott–Aldrich syndrome]]<br />
* [[Hyperimmunoglobulin E syndrome|Hyper-IgE syndrome]]<br />
<br />
| group3 = Other<br />
| list3 =<br />
* [[Common variable immunodeficiency]]<br />
* [[ICF syndrome]]<br />
<br />
}}<br />
<br />
| group2 = [[T cell deficiency]]<br/>([[T cell|T]])<br />
| list2 =<br />
* ''[[thymic hypoplasia]]:'' ''hypoparathyroid'' ([[DiGeorge syndrome|Di George's syndrome]])<br />
* ''euparathyroid'' ([[Nezelof syndrome]]<br />
* [[Ataxia–telangiectasia]])<br />
''peripheral:'' [[Purine nucleoside phosphorylase deficiency]]<br />
* [[Hyper IgM syndrome]] ([[Hyper-IgM syndrome type 1|1]])<br />
<br />
| group3 = [[Severe combined immunodeficiency|Severe]] [[Combined immunodeficiencies|combined]]<br/>(B+T)<br />
| list3 =<br />
* ''x-linked:'' [[X-linked severe combined immunodeficiency|X-SCID]]<br />''autosomal:'' [[Adenosine deaminase deficiency]]<br />
* [[Omenn syndrome]]<br />
* [[ZAP70 deficiency]]<br />
* [[Bare lymphocyte syndrome]]<br />
<br />
}}<br />
<br />
| group2 = [[Immunodeficiency#acquired|Acquired]]<br />
| list2 =<br />
* [[HIV/AIDS]]<br />
<br />
| group3 = [[Leukopenia]]:<br />[[Lymphocytopenia]]<br />
| list3 =<br />
* [[Idiopathic CD4+ lymphocytopenia]]<br />
<br />
| group4 = [[Complement deficiency|Complement<br/>deficiency]]<br />
| list4 =<br />
* ''[[C1-inhibitor]]'' ([[Angioedema]]/[[Hereditary angioedema]])<br />
* [[Complement 2 deficiency]]/[[Complement 4 deficiency]]<br />
* [[MBL deficiency]]<br />
* [[Properdin deficiency]]<br />
* [[Complement 3 deficiency]]<br />
* [[Terminal complement pathway deficiency]]<br />
* [[Paroxysmal nocturnal hemoglobinuria]]<br />
* [[Complement receptor deficiency]]<br />
<br />
}}<noinclude><br />
{{Documentation|content=<br />
{{Collapsible option}}<br />
[[Category:Immunology navigational boxes]]<br />
}}</noinclude></div>
Hutah