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Smithov-Lemliho-Opitzov syndróm
Č. záznamu d019082 Dátum 06.06.2025 Typ M - MESH Tematický termín Smithov-Lemliho-Opitzov syndróm MDT C16.131.077.860C16.320.565.398.850C16.320.565.925.875C18.452.584.500.937C18.452.584.563.850C18.452.648.398.850C18.452.648.925.875 Poznámka An autosomal recessive disorder of CHOLESTEROL metabolism. It is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. This syndrome is characterized by multiple CONGENITAL ABNORMALITIES, growth deficiency, and INTELLECTUAL DISABILITY. predmetové heslo
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