Difference between revisions of "Template:Inborn errors of purine–pyrimidine metabolism"
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imported>Arcadian (Mitochondrial neurogastrointestinal encephalopathy syndrome) |
imported>Was a bee m (→top: ICD code exported (from bot request)) |
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{{Navbox | {{Navbox | ||
− | | name = Inborn errors of | + | | name = Inborn errors of purine–pyrimidine metabolism |
− | | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of | + | | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of purine–pyrimidine metabolism|purine–pyrimidine metabolism]] |
+ | |listclass = hlist | ||
| state = {{{state|autocollapse}}} | | state = {{{state|autocollapse}}} | ||
− | |||
| group1 = [[Purine metabolism]] | | group1 = [[Purine metabolism]] | ||
− | | list1 = {{Navbox subgroup | + | | list1 = {{Navbox|subgroup |
| group1 = Anabolism | | group1 = Anabolism | ||
− | | list1 = [[Adenylosuccinate lyase deficiency]] | + | | list1 = |
+ | * [[Adenylosuccinate lyase deficiency]] | ||
+ | * [[Adenosine Monophosphate Deaminase Deficiency type 1]] | ||
| group2 = [[Nucleotide salvage]] | | group2 = [[Nucleotide salvage]] | ||
− | | list2 = [[Lesch–Nyhan | + | | list2 = |
+ | * [[Lesch–Nyhan syndrome]]/[[Hyperuricemia]] | ||
+ | * [[Adenine phosphoribosyltransferase deficiency]] | ||
| group3 = Catabolism | | group3 = Catabolism | ||
− | | list3 = [[Adenosine deaminase deficiency]] | + | | list3 = |
+ | * [[Adenosine deaminase deficiency]] | ||
+ | * [[Purine nucleoside phosphorylase deficiency]] | ||
+ | * [[Xanthinuria]] | ||
+ | * [[Gout]] | ||
+ | * [[Mitochondrial neurogastrointestinal encephalopathy syndrome]] | ||
}} | }} | ||
| group2 = [[Pyrimidine metabolism]] | | group2 = [[Pyrimidine metabolism]] | ||
− | | list2 = {{Navbox subgroup | + | | list2 = {{Navbox|subgroup |
| group1 = Anabolism | | group1 = Anabolism | ||
− | | list1 = [[Orotic aciduria]] | + | | list1 = |
+ | * [[Orotic aciduria]] | ||
+ | * [[Miller syndrome]] | ||
| group2 = Catabolism | | group2 = Catabolism | ||
− | | list2 = [[Dihydropyrimidine dehydrogenase deficiency]] | + | | list2 = |
+ | * [[Dihydropyrimidine dehydrogenase deficiency]] | ||
}} | }} | ||
− | |||
− | |||
− | |||
}}<noinclude> | }}<noinclude> | ||
− | [[Category:Inborn errors of metabolism]] | + | {{collapsible option}} |
− | [[Category:Metabolic disorder templates | + | [[Category:Inborn errors of purine-pyrimidine metabolism]] |
+ | [[Category:Metabolic disorder templates]] | ||
</noinclude> | </noinclude> |
Latest revision as of 21:28, 13 August 2020
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state=
parameter may be used:
|state=collapsed
:{{Inborn errors of purine–pyrimidine metabolism|state=collapsed}}
to show the template collapsed, i.e., hidden apart from its title bar|state=expanded
:{{Inborn errors of purine–pyrimidine metabolism|state=expanded}}
to show the template expanded, i.e., fully visible|state=autocollapse
:{{Inborn errors of purine–pyrimidine metabolism|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
.