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Concept information

disease > genetic disease > hereditary disease > familial dysalbuminemic hyperthyroxinemia
disease > endocrinopathy > thyroid diseases > familial dysalbuminemic hyperthyroxinemia

Terme préférentiel

familial dysalbuminemic hyperthyroxinemia  

Définition

  • Familial dysalbuminemic hyperthyroxinemia is a type of hyperthyroxinemia associated with mutations in the human serum albumin gene.The term was introduced in 1982. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-P6XNB1R1-2

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