Bevorzugtes Label : hyperbilirubinämie, hereditäre;
Ursprüngliche Kennung : D006933;
UMLS CUI : C0020435;
Manual NTBT mappings (CISMeF)
MeSH Descriptor(s) used for indexing
See also (suggested by CISMeF)
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=3111
2010
true
hyperbilirubinämie, hereditäre
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