Hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency

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;

Détails

Origin ID

617953;

UMLS CUI

C1840059;

CISMeF manual mappings
- hyperthyroxinemia due to decreased peripheral conversion of T4 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperthyroxinemia due to decreased peripheral conversion of T4 [MeSH concept]
- hyperthyroxinemia due to decreased peripheral conversion of T4 [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients