Home

             UMLS 2025

7/10

D006012

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.


Enter one or more words or parts of words

Click in last column to see ancestors descendants tree
Dict Code CUI Term Tree
Click on row column 3 or 4 for more information and multilingual
MSH D006012 C0017924 Deficiencies, Muscle Phosphorylase no pref
MSH D006012 C0017924 Disease, McArdle's no pref
MSH D006012 C0017924 Glycogen Storage Disease Type V preferred
MSH D006012 C0017924 Glycogenosis 5s no pref
MSH D006012 C0017924 McArdles Disease no pref
MSH D006012 C0017924 Muscle Phosphorylase Deficiencies no pref
MSH D006012 C0017924 Phosphorylase Deficiencies, Muscle no pref
MSH D006012 C0017924 Phosphorylase Deficiency, Muscle no pref
MSH D006012 C0017924 Disease, McArdle no pref
MSH D006012 C0017924 MCARDLE DIS no pref
MSH D006012 C0017924 MUSCLE PHOSPHORYLASE DEFIC no pref
MSH D006012 C0017924 GLYCOGEN STORAGE DIS V no pref
MSH D006012 C0017924 MCARDLES DIS no pref
MSH D006012 C0017924 DEFIC MUSCLE PHOSPHORYLASE no pref
MSHFIN D006012 C0017924 Glykogenoosi V preferred
MSHRUS D006012 C0017924 GLIKOGENOZ V TIPA no pref
MSHRUS D006012 C0017924 MIOFOSFORILAZNAIA NEDOSTATOCHNOST' no pref
MSHRUS D006012 C0017924 GLIKOGENA NAKOPLENIIA BOLEZN' V TIPA no pref
MSHRUS D006012 C0017924 MAK-ARDLA BOLEZN' no pref
MSHRUS D006012 C0017924 MAK-ARDLA-SHMIDTA-PIRSONA BOLEZN' no pref
MSHJPN D006012 C0017924 糖原病V型 preferred
MSHPOL D006012 C0017924 Niedobór fosforylazy mięśniowej no pref
MSHPOL D006012 C0017924 Glikogenoza typ V preferred
MSHCZE D006012 C0017924 glykogenóza typu V preferred
MSH D006012 C0017924 PYGM Deficiencies no pref
MSH D006012 C0017924 Deficiencies, PYGM no pref
MSH D006012 C0017924 Deficiency, PYGM no pref
MSHNOR D006012 C0017924 Glykogenlagringssykdom type 5 preferred
MSH D006012 C0017924 deficiencies, Myophosphorylase no pref
MSH D006012 C0017924 Syndromes, Mcardle no pref
MSH D006012 C0017924 Myophosphorylase deficiencies no pref
MSH D006012 C0017924 Mcardle Syndromes no pref
MSH D006012 C0017924 deficiency, Myophosphorylase no pref
MSH D006012 C0017924 Syndrome, Mcardle no pref
MSH D006012 C0017924 PYGM Deficiency no pref
MSH D006012 C0017924 Glycogenosis 5 no pref
MSH D006012 C0017924 Mcardle Syndrome no pref
MSH D006012 C0017924 Muscle Glycogen Phosphorylase Deficiency no pref
MSH D006012 C0017924 Muscle Phosphorylase Deficiency no pref
MSH D006012 C0017924 McArdle's Disease no pref
MSH D006012 C0017924 McArdle Type Glycogen Storage Disease no pref
MSH D006012 C0017924 Glycogen Storage Disease Type 5 no pref
MSH D006012 C0017924 McArdle Disease no pref
MSH D006012 C0017924 Glycogen Storage Disease V no pref
MSH D006012 C0017924 Deficiency, Muscle Phosphorylase no pref
MSH D006012 C0017924 Myophosphorylase deficiency no pref
MSHCZE D006012 C0017924 glykogenóza V no pref
MSHNOR D006012 C0017924 Glykogenlagringssykdom type V no pref
MSHNOR D006012 C0017924 Glykogenose 5 no pref
MSHFRE D006012 C0017924 Glycogénose de Mac Ardle no pref
MSHCZE D006012 C0017924 glykogenóza typ V no pref
MSHFRE D006012 C0017924 Maladie de McArdle no pref
MSHITA D006012 C0017924 Glicogenosi di tipo V no pref
MSHNOR D006012 C0017924 Myofosforylasemangel no pref
MSHSPA D006012 C0017924 Glucogenosis 5 no pref
MSHCZE D006012 C0017924 deficit svalové fosforylázy no pref
MSHFRE D006012 C0017924 Déficit en myophosphorylase no pref
MSHGER D006012 C0017924 McArdle-Krankheit no pref
MSHPOR D006012 C0017924 Glicogenose 5 no pref
MSHPOR D006012 C0017924 Doença de McArdle no pref
MSHFRE D006012 C0017924 Glycogénose de type 5 no pref
MSHCZE D006012 C0017924 glykogen - nemoc z ukládání typ V no pref
MSHFRE D006012 C0017924 Maladie de Mac Ardle no pref
MSHCZE D006012 C0017924 Syndrom McArdlův no pref
MSHCZE D006012 C0017924 McArdleho nemoc no pref
MSHFRE D006012 C0017924 Maladie de Mac Ardle-Schmid-Pearson no pref
MSHSPA D006012 C0017924 Enfermedad de McArdle no pref
MSHNOR D006012 C0017924 McArdles sykdom no pref
MSHCZE D006012 C0017924 McArdleho syndrom no pref
MSHCZE D006012 C0017924 nedostatek svalové fosforylázy no pref
MSHGER D006012 C0017924 Glykogenose V no pref
MSHPOR D006012 C0017924 Doença do Armazenamento de Glicogênio Tipo V no pref
MSHCZE D006012 C0017924 glykogenóza 5. typu no pref
MSHCZE D006012 C0017924 porucha ukládání glykogenu typu V no pref
MSHCZE D006012 C0017924 McArdleův syndrom no pref
MSHSWE D006012 C0017924 Myofosforylasbrist no pref
MSHSWE D006012 C0017924 Glykogenos 5 no pref
MSHSWE D006012 C0017924 Glykogenos typ V no pref
MSHSWE D006012 C0017924 McArdles sjukdom no pref
MSHSWE D006012 C0017924 Glykogeninlagringssjukdom typ V preferred
MSHGER D006012 C0017924 GLYKOGENOSE 05 no pref
MSHPOL D006012 C0017924 Zespół McArdle and 039;a no pref
MSHCZE D006012 C0017924 McArdleho choroba no pref
MSHCZE D006012 C0017924 McArdleova nemoc no pref
MSHCZE D006012 C0017924 McArdleova choroba no pref
MSHFRE D006012 C0017924 Glycogénose de type V preferred
MSHGER D006012 C0017924 Glykogenspeicherkrankheit Typ V preferred
MSHITA D006012 C0017924 Malattia da accumulo di glicogeno di tipo V preferred
MSHJPN D006012 C0017924 5型糖原病 no pref
MSHJPN D006012 C0017924 McArdle病 no pref
MSHJPN D006012 C0017924 マックアードル病 no pref
MSHJPN D006012 C0017924 糖原病5型 no pref
MSHJPN D006012 C0017924 McArdle-Schmid-Pearson病 no pref
MSHJPN D006012 C0017924 グリコーゲン病V型 no pref
MSHJPN D006012 C0017924 マッカードル-シュミット-ピアーソン病 no pref
MSHJPN D006012 C0017924 マッカードル・シュミット・ピアーソン病 no pref
MSHJPN D006012 C0017924 マッカードル病 no pref
MSHJPN D006012 C0017924 筋ホスホリラーゼ欠損性糖原病 no pref
MSHRUS D006012 C0017924 ГЛИКОГЕНА НАКОПЛЕНИЯ БОЛЕЗНЬ V ТИПА no pref
MSHRUS D006012 C0017924 ГЛИКОГЕНОЗ V ТИПА preferred
MSHRUS D006012 C0017924 МАК-АРДЛА БОЛЕЗНЬ no pref
MSHRUS D006012 C0017924 МАК-АРДЛА-ШМИДТА-ПИРСОНА БОЛЕЗНЬ no pref
MSHRUS D006012 C0017924 МИОФОСФОРИЛАЗНАЯ НЕДОСТАТОЧНОСТЬ no pref
MSHDUT D006012 C0017924 Glycogeenstapelingsziekte type V no pref
MSHDUT D006012 C0017924 Glycogenose type 5 no pref
MSHDUT D006012 C0017924 McArdle, ziekte van no pref
MSHDUT D006012 C0017924 Ziekte type V, glycogeenstapelings- preferred
MSHDUT D006012 C0017924 Myofosforylase deficiëntie no pref
MSHPOR D006012 C0017924 Doença de Depósito de Glicogênio Tipo V preferred
MSHSPA D006012 C0017924 Enfermedad del Almacenamiento de Glucógeno Tipo V no pref
D006012








Read more: https://www.nlm.nih.gov/research/umls/sourcereleasedocs/


Web development by Gayane Margaryan