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neuropatie amyloidné familiárne

Č. záznamu	d028227
Dátum	06.06.2025
Typ	M - MESH
Tematický termín	neuropatie amyloidné familiárne
Iný termín	Angličtina (Pseudonym) Familial Amyloid Polyneuropathies Slovenčina (Pseudonym) polyneuropatie amyloidové familiárne Slovenčina (Pseudonym) Wohlwill-Andradov syndróm Slovenčina (Pseudonym) Wohlwill-Corino Andradov syndróm
MDT	C10.574.500.050C10.668.829.050.050C16.320.400.050C16.320.565.176.050C18.452.648.176.050C18.452.845.500.050.050C18.452.845.500.075.050
Poznámka	Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.

predmetové heslo

Počet záznamov: 1