Talk:Adenosine Monophosphate Deaminase Deficiency type 1

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Requested move[edit]

The following discussion is an archived discussion of a requested move. Please do not modify it. Subsequent comments should be made in a new section on the talk page. No further edits should be made to this section.

The result of the move request was: page moved per request. I used the full name because the abbreviation seems to refer more to the gene itself, and not to the deficiency. - GTBacchus(talk) 03:15, 23 August 2011 (UTC)



Myoadenylate deaminase deficiencyAdenosine 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. url=http://ghr.nlm.nih.gov/gene/AMPD1 title=AMPD1 Gene url=http://ghr.nlm.nih.gov/condition/adenosine-monophosphate-deaminase-deficiency title=Adenosine monophosphate deaminase deficiency url=http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=458&Disease_Disease_Search_diseaseGroup=Adenosine-monophosphate-deaminase-deficiency&Disease_Disease_Search_diseaseType=Pat&Disease(s)/group of diseases=Adenosine-monophosphate-deaminase-deficiency&title=Adenosine-monophosphate-deaminase-deficiency&search=Disease_Search_Simple title=Adenosine monophosphate deaminase deficiency url=http://www.paliwoda.com/genotype/conditions/adenosinemonophosphatedeaminasedeficiency.html |title=Adenosine monophosphate deaminase deficiency Genotype Diagnostics 67.189.56.3 (talk) 02:59, 15 August 2011 (UTC)Tom

The above discussion is preserved as an archive of a requested move. Please do not modify it. Subsequent comments should be made in a new section on this talk page. No further edits should be made to this section.