Počet záznamov: 1
Fabryho choroba
Č. záznamu d000795 Dátum 06.06.2025 Typ M Tematický termín Fabryho choroba Iný termín Angličtina (Pseudonym) Anderson-Fabry Disease
Angličtina (Pseudonym) Angiokeratoma Corporis Diffusum
Slovenčina (Pseudonym) Andersonova-Fabryho choroba
Slovenčina (Pseudonym) angiokeratoma corporis diffusum
Slovenčina (Pseudonym) deficit alfa-galaktozidázy A
Slovenčina (Pseudonym) lipidóza dystopická hereditárna
Pozri tiež (Novšie záhlavie) alfa-galaktozidáza
(Skutočné meno) alfa-galaktozidáza
(Skutočné meno) ceramidy
(Novšie záhlavie) ceramidy
MDT C10.228.140.163.100.435.825.200C10.228.140.300.275.374C14.907.253.329.374C16.320.322.124C16.320.565.189.435.825.200C16.320.565.398.641.803.300C16.320.565.595.554.825.200C18.452.132.100.435.825.200C18.452.584.563.641.803.300C18.452.648.189.435.825.200C18.452.648.398.641.803.300C18.452.648.595.554.825.200 Poznámka An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. predmetové heslo
Počet záznamov: 1