Talk:Adenosine monophosphate deaminase deficiency type 1: Difference between revisions
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amended request |
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{{Requested move/dated|Adenosine Monophosphate Deaminase Deficiency type 1 (AMPD1)}} |
{{Requested move/dated|Adenosine Monophosphate Deaminase Deficiency type 1 (AMPD1)}} |
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[[Myoadenylate deaminase deficiency]] → [[Adenosine Monophosphate Deaminase Deficiency type 1 |
[[Myoadenylate deaminase deficiency]] → [[Adenosine Monophosphate Deaminase Deficiency type 1]] or [[AMPD1]] |
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The primary name for Myoadenlylate Deaminase Deficiency (MAD or MADD) has been changed in the last decade, as referenced below by |
The primary name for Myoadenlylate Deaminase Deficiency (MAD or MADD) has been changed in the last decade, as referenced below by Orphanet Rare Disease Research (36 countries are members) and US National Institutes of Health (NIH). |
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I should also state that Adenosine Monophosphate Deaminase, named [[/AMP_deaminase]] in Wiki is the gene that causes AMPD1 as well as AMPD2 and AMPD3, and this disease is also referenced there. Is the proper name for that page the abbreviation? or the full name? |
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Orphanet (Rare Disease Research) - 36 countries are members. |
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It would be nice if the two pages were standardized, and the next two diseases of AMPD could be added. |
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US National Institutes of Health (NIH). |
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See the following references. |
See the following references. |
Revision as of 05:33, 15 August 2011
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Requested move
![]() | It has been proposed in this section that Adenosine monophosphate deaminase deficiency type 1 be renamed and moved to Adenosine Monophosphate Deaminase Deficiency type 1 (AMPD1). A bot will list this discussion on the requested moves current discussions subpage within an hour of this tag being placed. The discussion may be closed 7 days after being opened, if consensus has been reached (see the closing instructions). Please base arguments on article title policy, and keep discussion succinct and civil. Please use {{subst:requested move}} . Do not use {{requested move/dated}} directly. |
Myoadenylate deaminase deficiency → Adenosine Monophosphate Deaminase Deficiency type 1 or AMPD1
The primary name for Myoadenlylate Deaminase Deficiency (MAD or MADD) has been changed in the last decade, as referenced below by Orphanet Rare Disease Research (36 countries are members) and US National Institutes of Health (NIH). I should also state that Adenosine Monophosphate Deaminase, named /AMP_deaminase in Wiki is the gene that causes AMPD1 as well as AMPD2 and AMPD3, and this disease is also referenced there. Is the proper name for that page the abbreviation? or the full name? It would be nice if the two pages were standardized, and the next two diseases of AMPD could be added.
See the following references.
[1]
[2]
Cite error: A <ref>
tag is missing the closing </ref>
(see the help page).
67.189.56.3 (talk) 02:59, 15 August 2011 (UTC)Tom
- ^ {cite web |url=http://ghr.nlm.nih.gov/gene/AMPD1 |title=AMPD1 Gene]]
- ^ {cite web |url=http://ghr.nlm.nih.gov/condition/adenosine-monophosphate-deaminase-deficiency |title=Adenosine monophosphate deaminase deficiency}}