Preferred Label : Hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency;
Type : Other, mainly phenotypes with suspected mendelian basis;
Alternative titles and symbols : Hyperthyroxinemia, euthyroid, due to decreased peripheral conversion of t4;
Prefixed ID : 617953;
Origin ID : 617953;
UMLS CUI : C1840059;
CISMeF manual mappings
Semantic type(s)
UMLS correspondences (same concept)