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gangliozidózy GM2
Č. záznamu d020143 Dátum 06.06.2025 Typ M Tematický termín gangliozidózy GM2 Iný termín Angličtina (Pseudonym) G(M2) Gangliosidoses
Slovenčina (Pseudonym) G(M2) gangliozidózy
Pozri tiež (Skutočné meno) beta-N-acetylhexozaminidázy
MDT C10.228.140.163.100.435.825.300.300C16.320.565.189.435.825.300.300C16.320.565.398.641.803.350.300C16.320.565.595.554.825.300.300C18.452.132.100.435.825.300.300C18.452.584.563.641.803.350.300C18.452.648.189.435.825.300.300C18.452.648.398.641.803.350.300C18.452.648.595.554.825.300.300 Poznámka A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS. predmetové heslo
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