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D000795

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 D000795 C0002986 Anderson Fabry Disease no pref
MSH D000795 C0002986 Fabry Disease preferred
MSH D000795 C0002986 alpha Galactosidase A Deficiency Disease no pref
MSHSWE D000795 C0002986 Fabrys sjukdom preferred
MSH D000795 C0002986 ALPHA GALACTOSIDASE A DEFIC DIS no pref
MSH D000795 C0002986 FABRY DIS no pref
MSHCZE D000795 C0002986 Fabryho nemoc preferred
MSHFIN D000795 C0002986 Fabryn tauti preferred
MSHRUS D000795 C0002986 ANDERSONA-FABRI BOLEZN' no pref
MSHRUS D000795 C0002986 FABRI BOLEZN' no pref
MSHRUS D000795 C0002986 ANGIOKERATOMA TULOVISHCHA DIFFUZNAIA no pref
MSHJPN D000795 C0002986 Fabry病 preferred
MSH D000795 C0002986 alpha Galactosidase A Deficiency no pref
MSH D000795 C0002986 Deficiency, alpha-Galactosidase A no pref
MSHPOL D000795 C0002986 Glikosfingolipidoza no pref
MSH D000795 C0002986 Lipidosis, Hereditary Dystopic no pref
MSH D000795 C0002986 Diffuse Angiokeratoma no pref
MSH D000795 C0002986 Deficiency, Ceramide Trihexosidase no pref
MSHNOR D000795 C0002986 Fabrys sykdom preferred
MSH D000795 C0002986 Deficiency, GLA no pref
MSH D000795 C0002986 Angiokeratoma, Diffuse no pref
MSH D000795 C0002986 alpha-Galactosidase A Deficiency Disease no pref
MSH D000795 C0002986 Fabry's Disease preferred
MSH D000795 C0002986 Hereditary Dystopic Lipidosis no pref
MSH D000795 C0002986 Angiokeratoma Corporis Diffusum no pref
MSH D000795 C0002986 GLA Deficiency no pref
MSH D000795 C0002986 Anderson-Fabry Disease no pref
MSH D000795 C0002986 Angiokeratoma Diffuse no pref
MSH D000795 C0002986 Ceramide Trihexosidase Deficiency no pref
MSH D000795 C0002986 alpha-Galactosidase A Deficiency no pref
MSHNOR D000795 C0002986 Arvelig dystopisk lipidose med alfagalaktosidase A-mangel no pref
MSHCZE D000795 C0002986 angiokeratoma corporis diffusum no pref
MSHFRE D000795 C0002986 Angiokératose diffuse universelle no pref
MSHGER D000795 C0002986 Fabry-Anderson-Syndrom no pref
MSHFRE D000795 C0002986 Déficit en alpha-galactosidase A no pref
MSHSPA D000795 C0002986 Enfermedad de Anderson-Fabry no pref
MSHCZE D000795 C0002986 Andersonova-Fabryho nemoc no pref
MSHGER D000795 C0002986 Angiokeratoma corporis diffusum no pref
MSHPOR D000795 C0002986 Angioceratoma Corpóreo Difuso no pref
MSHFRE D000795 C0002986 Thésaurismose lipoïdique héréditaire no pref
MSHPOR D000795 C0002986 Doença de Anderson-Fabry no pref
MSHSPA D000795 C0002986 Angioqueratoma Corpóreo Difuso no pref
MSHCZE D000795 C0002986 Fabryho syndrom no pref
MSHFRE D000795 C0002986 Angiokératome diffus de Fabry no pref
MSHFRE D000795 C0002986 Angiokératose diffuse de Fabry no pref
MSHFRE D000795 C0002986 Sphingolipidose héréditaire de Fabry no pref
MSHRUS D000795 C0002986 ФАБРИ БОЛЕЗНЬ preferred
MSHRUS D000795 C0002986 АНГИОКЕРАТОМА ТУЛОВИЩА ДИФФУЗНАЯ no pref
MSHRUS D000795 C0002986 АНГИОКЕРАТОМА ДИФФУЗНАЯ no pref
MSHRUS D000795 C0002986 ANGIOKERATOMA DIFFUZNAIA no pref
MSHCZE D000795 C0002986 difuzní angiokeratom no pref
MSHCZE D000795 C0002986 deficit alfa-galaktosidázy A no pref
MSHCZE D000795 C0002986 X-vázaná sfingolipidóza no pref
MSHCZE D000795 C0002986 deficience alfa-galaktosidázy A no pref
MSHCZE D000795 C0002986 Fabryho choroba no pref
MSHCZE D000795 C0002986 deficit alfa-galaktosidasy A no pref
MSHPOR D000795 C0002986 Deficiência de alfa-Galactosidase A no pref
MSHPOR D000795 C0002986 Angioceratoma Difuso no pref
MSHPOL D000795 C0002986 Choroba Andersona-Fabry and 039;ego no pref
MSHPOL D000795 C0002986 Choroba Fabry and 039;ego preferred
MSHFRE D000795 C0002986 Maladie de Fabry preferred
MSHGER D000795 C0002986 Fabry-Krankheit preferred
MSHITA D000795 C0002986 Malattia di Fabry preferred
MSHJPN D000795 C0002986 Anderson-Fabry病 no pref
MSHJPN D000795 C0002986 α-ガラクトシダーゼ欠損症 no pref
MSHJPN D000795 C0002986 びまん性体幹角化血管腫 no pref
MSHJPN D000795 C0002986 びまん性体部被角血管腫 no pref
MSHJPN D000795 C0002986 びまん性体部角化血管腫 no pref
MSHJPN D000795 C0002986 び慢性体部被角血管腫 no pref
MSHJPN D000795 C0002986 セラミドトリヘキソシド蓄積症 no pref
MSHJPN D000795 C0002986 ファブリ病 no pref
MSHJPN D000795 C0002986 広汎性体幹角化血管腫 no pref
MSHJPN D000795 C0002986 瀰漫性体幹角化血管腫 no pref
MSHJPN D000795 C0002986 糖脂質リピドーシス no pref
MSHJPN D000795 C0002986 角化血管腫-瀰漫性体幹 no pref
MSHJPN D000795 C0002986 び漫性体幹被角血管腫 no pref
MSHJPN D000795 C0002986 アンダーソン-ファブリー病 no pref
MSHJPN D000795 C0002986 ガラクトシダーゼ欠損症-アルファ no pref
MSHJPN D000795 C0002986 ファブリー病 no pref
MSHJPN D000795 C0002986 角化血管腫-びまん性体幹 no pref
MSHRUS D000795 C0002986 АНДЕРСОНА-ФАБРИ БОЛЕЗНЬ no pref
MSHDUT D000795 C0002986 Angiokeratoma corporis diffusum preferred
MSHDUT D000795 C0002986 Fabry, ziekte van no pref
MSHDUT D000795 C0002986 Ziekte van Fabry no pref
MSHDUT D000795 C0002986 Ziekte van Fabry-Anderson no pref
MSHPOR D000795 C0002986 Doença de Fabry preferred
MSHSPA D000795 C0002986 Enfermedad de Fabry no pref
D000795








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