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D006009

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 D006009 C0017921 Glycogen Storage Disease Type II preferred
MSH D006009 C0017921 Glycogenosis, Generalized no pref
MSH D006009 C0017921 Pompes Disease no pref
MSH D006009 C0017921 GLYCOGEN STORAGE DIS II no pref
MSH D006009 C0017921 DEFIC DIS ACID MALTASE no pref
MSH D006009 C0017921 POMPE DIS no pref
MSH D006009 C0017921 POMPES DIS no pref
MSH D006009 C0017921 ACID MALTASE DEFIC DIS no pref
MSH D006009 C0017921 LYSOSOMAL ALPHA 1 4 GLUCOSIDASE DEFIC DIS no pref
MSH D006009 C0017921 DEFIC DIS LYSOSOMAL ALPHA 1 4 GLUCOSIDASE no pref
MSHFIN D006009 C0017921 Glykogenoosi II preferred
MSHRUS D006009 C0017921 POMPE BOLEZN' no pref
MSHRUS D006009 C0017921 GLIKOGENOZ II TIPA no pref
MSHRUS D006009 C0017921 GENERALIZOVANNYI GLIKOGENOZ no pref
MSHRUS D006009 C0017921 GLIKOGENA NAKOPLENIIA BOLEZN' II TIPA no pref
MSH D006009 C0017921 Type II, Glycogenosis no pref
MSH D006009 C0017921 Generalized Glycogenoses no pref
MSH D006009 C0017921 Glycogenoses, Generalized no pref
MSH D006009 C0017921 Disease, Pompe's no pref
MSH D006009 C0017921 Disease, Pompe no pref
MSHPOL D006009 C0017921 Glikogenoza typ II preferred
MSHPOL D006009 C0017921 Glikogenoza uogólniona no pref
MSHPOL D006009 C0017921 Choroba Pompego no pref
MSH D006009 C0017921 Lysosomal alpha 1,4 Glucosidase Deficiency Disease no pref
MSH D006009 C0017921 Type IIs, Glycogenosis no pref
MSHCZE D006009 C0017921 glykogenóza typu II preferred
MSHNOR D006009 C0017921 Pompes sykdom preferred
MSH D006009 C0017921 Deficiencies, Acid Alpha-Glucosidase no pref
MSH D006009 C0017921 Deficiency, GAA no pref
MSH D006009 C0017921 Acid Alpha Glucosidase Deficiency no pref
MSH D006009 C0017921 Alpha-Glucosidase Deficiencies, Acid no pref
MSH D006009 C0017921 Alpha-Glucosidase Deficiency, Acid no pref
MSH D006009 C0017921 Deficiencies, GAA no pref
MSH D006009 C0017921 GAA Deficiencies no pref
MSH D006009 C0017921 Acid Alpha-Glucosidase Deficiencies no pref
MSH D006009 C0017921 Deficiency, Acid Alpha-Glucosidase no pref
MSH D006009 C0017921 Alpha-Glucosidase Deficiencies no pref
MSH D006009 C0017921 Deficiency of Alpha Glucosidase no pref
MSH D006009 C0017921 GSD2s no pref
MSH D006009 C0017921 Alpha-Glucosidase Deficiency no pref
MSH D006009 C0017921 Glycogen Storage Disease Type 2 no pref
MSH D006009 C0017921 Acid Maltase Deficiency Disease no pref
MSH D006009 C0017921 Generalized Glycogenosis no pref
MSH D006009 C0017921 Lysosomal alpha-1,4-Glucosidase Deficiency Disease no pref
MSH D006009 C0017921 GSD2 no pref
MSH D006009 C0017921 Deficiency Disease, Lysosomal alpha-1,4-Glucosidase no pref
MSH D006009 C0017921 GSD II no pref
MSH D006009 C0017921 Deficiency Disease, Acid Maltase no pref
MSH D006009 C0017921 Pompe's Disease no pref
MSH D006009 C0017921 Deficiency of Alpha-Glucosidase no pref
MSH D006009 C0017921 Glycogenosis Type II no pref
MSH D006009 C0017921 Glycogen Storage Disease II no pref
MSH D006009 C0017921 Pompe Disease no pref
MSH D006009 C0017921 Glycogenosis 2 no pref
MSH D006009 C0017921 Acid Alpha-Glucosidase Deficiency no pref
MSH D006009 C0017921 GAA Deficiency no pref
MSHGER D006009 C0017921 Lysosomale alpha-1,4-Glukosidase-Mangelkrankheit no pref
MSHFRE D006009 C0017921 Maladie de Pompe no pref
MSHNOR D006009 C0017921 Glykogenavleiringssykdom type II no pref
MSHPOR D006009 C0017921 Doença da Deficiência de alfa-1,4-Glucosidase Lisossômica no pref
MSHSPA D006009 C0017921 Glucogenosis 2 no pref
MSHGER D006009 C0017921 Pompe-Krankheit no pref
MSHPOR D006009 C0017921 Doença do Armazenamento de Glicogênio Tipo II no pref
MSHFRE D006009 C0017921 Déficit en alpha-1,4-glucosidase acide lysosomiale no pref
MSHGER D006009 C0017921 Glykogenose II no pref
MSHSPA D006009 C0017921 Deficiencia de Maltasa Ácida no pref
MSHSPA D006009 C0017921 Enfermedad por Deficiencia de Lisosoma alfa-1,4-Glucosidasa no pref
MSHPOR D006009 C0017921 Doença da Deficiência de Maltase Ácida no pref
MSHCZE D006009 C0017921 nemoc z nedostatku kyselé maltázy no pref
MSHNOR D006009 C0017921 Glykogenavleiringssykdom type 2 no pref
MSHCZE D006009 C0017921 generalizovaná glykogenóza no pref
MSHPOR D006009 C0017921 Glicogenose 2 no pref
MSHSPA D006009 C0017921 Enfermedad por Deficiencia de Maltasa Ácida no pref
MSHPOR D006009 C0017921 Glicogenose Generalizada no pref
MSHFRE D006009 C0017921 Déficit en alpha-1,4-glucosidase acide lysosomale no pref
MSHNOR D006009 C0017921 Glykogenose type 2 no pref
MSHCZE D006009 C0017921 Pompeho choroba no pref
MSHPOR D006009 C0017921 Deficiência de Maltase Ácida no pref
MSHPOR D006009 C0017921 Doença de Pompe no pref
MSHITA D006009 C0017921 Malattia di Pompe no pref
MSHCZE D006009 C0017921 Pompeho nemoc no pref
MSHFRE D006009 C0017921 Déficit en alpha-1,4-glucosidase acide no pref
MSHGER D006009 C0017921 Morbus Pompe no pref
MSHFRE D006009 C0017921 Glycogénose de Pompe no pref
MSHGER D006009 C0017921 Saure-Maltase-Mangelkrankheit no pref
MSHFRE D006009 C0017921 Glycogénose de type 2 no pref
MSHSPA D006009 C0017921 Glucogenosis Generalizada no pref
MSHNOR D006009 C0017921 Glykogenose type II no pref
MSHSPA D006009 C0017921 Enfermedad de Pompe no pref
MSHCZE D006009 C0017921 glykogen - nemoc z ukládání typ II no pref
MSHFRE D006009 C0017921 Déficit en maltase acide no pref
MSHFRE D006009 C0017921 GSD II no pref
MSHGER D006009 C0017921 Generalisierte Glykogenose no pref
MSHITA D006009 C0017921 Glicogenosi di tipo II no pref
MSHCZE D006009 C0017921 GSD2 no pref
MSHCZE D006009 C0017921 deficit GAA no pref
MSHCZE D006009 C0017921 glykogenóza II no pref
MSHCZE D006009 C0017921 GSD II no pref
MSHSWE D006009 C0017921 Glykogenos typ II no pref
MSHSWE D006009 C0017921 Glykogeninlagringssjukdom typ II preferred
MSHSWE D006009 C0017921 Glykogenos 2 no pref
MSHSWE D006009 C0017921 Pompes sjukdom no pref
MSHGER D006009 C0017921 Lysosomale alpha 01 04 Glukosidase Mangelkrankheit no pref
MSHGER D006009 C0017921 GLYKOGENOSE 02 no pref
MSHGER D006009 C0017921 Glykogenspeicherkrankheit Typ II preferred
MSHITA D006009 C0017921 Malattia da accumulo di glicogeno di tipo II preferred
MSHRUS D006009 C0017921 ГЕНЕРАЛИЗОВАННЫЙ ГЛИКОГЕНОЗ no pref
MSHRUS D006009 C0017921 ГЛИКОГЕНА НАКОПЛЕНИЯ БОЛЕЗНЬ II ТИПА no pref
MSHRUS D006009 C0017921 ГЛИКОГЕНОЗ II ТИПА preferred
MSHRUS D006009 C0017921 ПОМПЕ БОЛЕЗНЬ no pref
MSHDUT D006009 C0017921 Gegeneraliseerde glycogenose preferred
MSHDUT D006009 C0017921 Glycogeenstapelingsziekte type II no pref
MSHDUT D006009 C0017921 Glycogenose type 2 no pref
MSHDUT D006009 C0017921 Pompe, ziekte van no pref
MSHDUT D006009 C0017921 Ziekte type II, glycogeenstapelings- no pref
MSHDUT D006009 C0017921 Lysosomale alfa-1,4-glucosidasedeficiëntieziekte no pref
MSHDUT D006009 C0017921 Zure-maltasedeficiëntieziekte no pref
MSHPOR D006009 C0017921 Doença de Depósito de Glicogênio Tipo II preferred
MSHFRE D006009 C0017921 Glycogénose de type II preferred
MSHSPA D006009 C0017921 Enfermedad del Almacenamiento de Glucógeno Tipo II no pref
MSHCZE D006009 C0342751 deficit kyselé maltázy preferred
MSHNOR D006009 C0342751 Sur maltase-mangel preferred
MSHCZE D006009 C0342751 deficit alfa-1,4-glukozidázy no pref
MSHCZE D006009 C0342751 deficit alfa-1,4-glukosidázy no pref
MSHSWE D006009 C0342751 Surt maltasbrist preferred
MSH D006009 C0751172 GYLCOGEN STORAGE DIS TYPE II ADULT no pref
MSH D006009 C0751172 ADULT GLYCOGEN STORAGE DIS TYPE II no pref
MSHFRE D006009 C0751172 Glycogénose de type II de l'adulte preferred
MSHNOR D006009 C0751172 Adult glykogenavleiringssykdom type 2 preferred
MSH D006009 C0751172 Adult Glycogen Storage Disease Type II preferred
MSH D006009 C0751172 Glycogen Storage Disease Type II, Adult preferred
MSHNOR D006009 C0751172 Adult glykogenavleiringssykdom type II no pref
MSHNOR D006009 C0751172 Glykogenavleiringssykdom type 2, debut voksen alder no pref
MSHNOR D006009 C0751172 Glykogenavleiringssykdom type II, debut voksen alder no pref
MSHFRE D006009 C0751172 Glycogénose de type 2 de l'adulte no pref
MSHCZE D006009 C0751172 glykogenóza typu II, adultní forma preferred
MSH D006009 C0751173 INFANTILE GLYCOGEN STORAGE DIS TYPE II no pref
MSH D006009 C0751173 GLYCOGEN STORAGE DIS TYPE II INFANTILE no pref
MSHFRE D006009 C0751173 Glycogénose de type II infantile preferred
MSHNOR D006009 C0751173 Infantil glykogenavleiringssykdom type 2 preferred
MSH D006009 C0751173 Infantile Glycogen Storage Disease Type II preferred
MSH D006009 C0751173 Glycogen Storage Disease Type II, Infantile preferred
MSHNOR D006009 C0751173 Infantil glykogenavleiringssykdom type II no pref
MSHNOR D006009 C0751173 Glykogenavleiringssykdom type II, debut spedbarnsalder no pref
MSHFRE D006009 C0751173 Glycogénose de type 2 infantile no pref
MSHNOR D006009 C0751173 Glykogenavleiringssykdom type 2, debut spedbarnsalder no pref
MSHCZE D006009 C0751173 glykogenóza typu II, infantilní forma preferred
MSH D006009 C0751174 GLYCOGEN STORAGE DIS TYPE II JUVENTILE no pref
MSH D006009 C0751174 JUVENILE GLYCOGEN STORAGE DIS TYPE II no pref
MSHFRE D006009 C0751174 Glycogénose de type II juvénile preferred
MSHNOR D006009 C0751174 Juvenil glykogenavleiringssykdom type 2 preferred
MSH D006009 C0751174 Glycogen Storage Disease Type II, Juvenile preferred
MSH D006009 C0751174 Juvenile Glycogen Storage Disease Type II preferred
MSHNOR D006009 C0751174 Glykogenavleiringssykdom type 2, debut ungdomsalder no pref
MSHNOR D006009 C0751174 Glykogenavleiringssykdom type II, debut ungdomsalder no pref
MSHFRE D006009 C0751174 Glycogénose de type 2 juvénile no pref
MSHNOR D006009 C0751174 Juvenil glykogenavleiringssykdom type II no pref
MSHCZE D006009 C0751174 glykogenóza typu II, juvenilní forma preferred
MSH D006009 C5700101 Deficiency, Acid Maltase preferred
MSH D006009 C5700101 Alpha-1,4-Glucosidase Deficiencies no pref
MSH D006009 C5700101 Acid Maltase Deficiencies preferred
MSH D006009 C5700101 Maltase Deficiencies, Acid preferred
MSH D006009 C5700101 Deficiencies, Alpha-1,4-Glucosidase no pref
MSH D006009 C5700101 Alpha 1,4 Glucosidase Deficiency no pref
MSH D006009 C5700101 Deficiencies, Acid Maltase preferred
MSH D006009 C5700101 Deficiency, Alpha-1,4-Glucosidase no pref
MSH D006009 C5700101 Alpha-1,4-Glucosidase Deficiency no pref
MSH D006009 C5700101 Acid Maltase Deficiency preferred
D006009








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