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GENATLAS PHENOTYPE

last update : 06-12-2017

Symbol	FDAH
Location	4q13.3
Name	familial dysalbuminemic hyperthyroxinemia
Corresponding gene	ALB
Main clinical features	characterized by the presence of a variant serum albumin with preferential affinity for thyroxine (T4) in clinically euthyroid individuals elevated total T4 and elevated or normal free T4 values with normal TSH levels
Genetic determination	autosomal dominant
Function/system disorder	endocrinology
Type	disease

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