Skip navigation

Disease Hyperthyroxinemia, Familial Dysalbuminemic

Name Hyperthyroxinemia, Familial Dysalbuminemic
Synonyms Dysalbuminemic Hyperthyroxinemia, Familial | EUTHYROID HYPERTHYROXINEMIA 1 | Familial Dysalbuminemic Hyperthyroxinemia | FDAH | FDH
Definition An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum THYROXINE; (T4) in euthyroid patients with abnormal SERUM ALBUMIN that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and TSH are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the ALB gene on CHROMOSOME 4.
Categories Endocrine system disease | Genetic disease (inborn)
MeSH® ID D050010
OMIM® ID 615999

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Hyperthyroxinemia, Familial Dysalbuminemic Has associated chemicals Has associated genes
2. DiseasesEndocrine System Diseases Has associated chemicals Has associated genes Has associated exposure references Thyroid Diseases Has associated chemicals Has associated genes Has associated exposure references Hyperthyroxinemia Has associated chemicals Has associated genes Hyperthyroxinemia, Familial Dysalbuminemic Has associated chemicals Has associated genes

Top ↑ Descendants

Hyperthyroxinemia, Familial Dysalbuminemic Has associated chemicals Has associated genes
  Dysalbuminemic Hyperthyroxinemia