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D018980

We use MeSH codes primarily for indexing, cataloging, and searching biomedical literature.
MSH Medical Subject Headings The original, English version of the vocabulary.
MSHPOR Portuguese Portuguese MeSH headings.
MSHSPA Spanish (Decs) Spanish MeSH headings (often referenced as DeCS—Descriptors in Health Sciences).
MSHRUS Russian Russian MeSH headings.
MSHITA Italian Italian MeSH headings.
MSHGER German German MeSH headings.
MSHFRE French French MeSH headings.
MSHSWE Swedish Swedish MeSH headings.
MSHCZE Czech Czech MeSH headings.
MSHFIN Finnish Finnish MeSH headings.
MSHJPN Japanese Japanese MeSH headings.
MSHLAV Latvian Latvian MeSH headings.
MSHSCR Serbo-Croatian Serbo-Croatian MeSH headings.
MSHPOL Polish Polish MeSH headings.
MSHNOR Norwegian Norwegian MeSH headings.
MSHDUT Dutch Dutch MeSH headings.


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Dict Code CUI Term Tree
Click on row column 3 or 4 for more information and multilingual
MSH D018980 C0175702 Syndrome, Williams preferred
MSH D018980 C0175702 Syndrome, Williams-Beuren no pref
MSH D018980 C0175702 Williams Beuren Syndrome no pref
MSH D018980 C0175702 Williams Syndrome preferred
MSHSWE D018980 C0175702 Williams syndrom preferred
MSHCZE D018980 C0175702 Williamsův-Beurenův syndrom preferred
MSHFIN D018980 C0175702 Williamsin oireyhtymä preferred
MSHRUS D018980 C0175702 EL'FA LITSA SINDROM no pref
MSHRUS D018980 C0175702 UIL'IAMSA SINDROM no pref
MSHRUS D018980 C0175702 BOIRENA SINDROM no pref
MSHRUS D018980 C0175702 UIL'IAMSA-BOIRENA SINDROM no pref
MSHJPN D018980 C0175702 Williams症候群 preferred
MSHPOL D018980 C0175702 Zespół Williamsa preferred
MSHPOL D018980 C0175702 Zespół twarzy elfa no pref
MSHPOL D018980 C0175702 Zespół Williamsa-Beurena no pref
MSHJPN D018980 C0175702 ウィリアムズ症候群 no pref
MSHJPN D018980 C0175702 ウィリアムズ-ビューレン症候群 no pref
MSHNOR D018980 C0175702 Williams' syndrom preferred
MSH D018980 C0175702 Stenoses, Hypercalcemia-Supravalvar Aortic no pref
MSH D018980 C0175702 Aortic Stenosis, Hypercalcemia-Supravalvar no pref
MSH D018980 C0175702 Syndrome, Beuren no pref
MSH D018980 C0175702 Hypercalcemia Supravalvar Aortic Stenosis no pref
MSH D018980 C0175702 Stenosis, Hypercalcemia-Supravalvar Aortic no pref
MSH D018980 C0175702 Aortic Stenoses, Hypercalcemia-Supravalvar no pref
MSH D018980 C0175702 Hypercalcemia-Supravalvar Aortic Stenoses no pref
MSH D018980 C0175702 Beuren Syndrome no pref
MSH D018980 C0175702 Hypercalcemia-Supravalvar Aortic Stenosis no pref
MSH D018980 C0175702 Williams Contiguous Gene Syndrome no pref
MSH D018980 C0175702 Supravalvar Aortic Stenosis Syndrome no pref
MSH D018980 C0175702 Contiguous Gene Syndrome, Williams no pref
MSH D018980 C0175702 Chromosome 7q11.23 Deletion Syndrome no pref
MSH D018980 C0175702 Williams-Beuren Syndrome no pref
MSHSPA D018980 C0175702 Síndrome de Facie de Duende no pref
MSHFRE D018980 C0175702 Syndrome de Williams-Beuren no pref
MSHSPA D018980 C0175702 Síndrome de Williams de Gen Contiguo no pref
MSHITA D018980 C0175702 Sindrome di Williams-Beuren no pref
MSHFRE D018980 C0175702 Syndrome de Williams et Beuren no pref
MSHNOR D018980 C0175702 Alveansiktssyndrom no pref
MSHCZE D018980 C0175702 Williamsův syndrom no pref
MSHFRE D018980 C0175702 Syndrome de la face d'elfe no pref
MSHFRE D018980 C0175702 Syndrome des gènes contigus de Williams no pref
MSHPOR D018980 C0175702 Síndrome do Gene Contíguo de Williams no pref
MSHPOR D018980 C0175702 Síndrome de Fácies de Elfo no pref
MSHNOR D018980 C0175702 Williams-Beurens syndrom no pref
MSHFRE D018980 C0175702 Syndrome de délétion chromosomique 7q11.23 no pref
MSHGER D018980 C0175702 Elfengesicht-Syndrom no pref
MSHGER D018980 C0175702 Williams-Beuren-Syndrom no pref
MSHNOR D018980 C0175702 Elfin facies-syndrom no pref
MSHFRE D018980 C0175702 Syndrome du faciès d'elfe no pref
MSHCZE D018980 C0175702 Williams-Beurenův syndrom no pref
MSHSWE D018980 C0175702 William-Beurens syndrom no pref
MSHSWE D018980 C0175702 Elfin face syndrom no pref
MSHGER D018980 C0175702 Williams-Syndrom preferred
MSHITA D018980 C0175702 Sindrome di Williams preferred
MSHJPN D018980 C0175702 Williams-Beuren症候群 no pref
MSHJPN D018980 C0175702 ウィリアムス症候群 no pref
MSHJPN D018980 C0175702 ウイリアムズ症候群 no pref
MSHJPN D018980 C0175702 妖精顔貌症候群 no pref
MSHJPN D018980 C0175702 ウィリアムス-ビューレン症候群 no pref
MSHRUS D018980 C0175702 БОЙРЕНА СИНДРОМ no pref
MSHRUS D018980 C0175702 УИЛЬЯМСА-БОЙРЕНА СИНДРОМ no pref
MSHRUS D018980 C0175702 УИЛЬЯМСА СИНДРОМ preferred
MSHRUS D018980 C0175702 ЭЛЬФА ЛИЦА СИНДРОМ no pref
MSHDUT D018980 C0175702 Contiguous-gene syndrome, Williams no pref
MSHDUT D018980 C0175702 Elfengelaat no pref
MSHDUT D018980 C0175702 Elfjesgezicht no pref
MSHDUT D018980 C0175702 Syndroom, Williams- preferred
MSHDUT D018980 C0175702 Williams-syndroom no pref
MSHPOR D018980 C0175702 Síndrome de Williams preferred
MSHFRE D018980 C0175702 Syndrome de Williams preferred
MSHSPA D018980 C0175702 Síndrome de Williams no pref
D018980








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