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DeCS
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Descriptor Inglés:
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Hereditary Complement Deficiency Diseases
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Descriptor Español:
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Enfermedades por Deficiencia de Complemento Hereditario
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Descriptor Portugués:
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Doenças da Deficiência Hereditária de Complemento
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Sinónimos Inglés:
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Complement Deficiencies
Complement Deficiency
Inherited Complement Deficiency Diseases
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Categoría:
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C16.320.798.500
C20.673.795.500
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Definición Inglés:
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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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Nota Histórica Inglés:
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2020
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Calificadores Permitidos Inglés:
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Número del Registro:
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59119
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Identificador Único:
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D000081208
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Ocurrencia en la BVS:
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Similar:
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DeCS
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