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choroby z deficitu komplementu, dedičné

Č. záznamu	d000081208
Dátum	06.06.2025
Typ	M - MESH
Tematický termín	choroby z deficitu komplementu, dedičné
Iný termín	Angličtina (Pseudonym) Complement Deficiencies Angličtina (Pseudonym) Inherited Complement Deficiency Diseases Slovenčina (Pseudonym) ochorenia spôsobené deficitom komplementu Slovenčina (Pseudonym) deficit komplementu Slovenčina (Pseudonym) nedostatok komplementu
MDT	C16.320.798.500C20.673.795.500
Poznámka	Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).

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Počet záznamov: 1