Descriptors Found: 1
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Descriptor English:   Hyperthyroxinemia, Familial Dysalbuminemic 
Descriptor Spanish:   Hipertiroxinemia Disalbuminémica Familiar 
Descriptor Portuguese:   Hipertireoxinemia Disalbuminêmica Familiar 
Synonyms English:   Dysalbuminemic Hyperthyroxinemia, Familial
Familial Dysalbuminemic Hyperthyroxinemia  
Tree Number:   C16.320.427
Definition English:   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. 
History Note English:   2006 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   50510 
Unique Identifier:   D050010 

Occurrence in VHL: