Hyperthyroxinemia, Familial Dysalbuminemic [familiární dysalbuminemická hypertyroxinemie]

topical
2
Terms

hypertyroxinémie familiární dysalbuminemická

 

Familial Dysalbuminemic Hyperthyroxinemia

Persistent link   https://www.medvik.cz/link/D050010
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.

DUI
D050010 MeSH Browser
CUI
M0471943
Previous indexing
Serum Albumin (1982-2005); Thyroxine (1982-2005)
History note
2006
Public note
2006

C Diseases
C16.320.051 Alagille Syndrome 19
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.365 Hemoglobinopathies 68
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.540 Marfan Syndrome 105
C16.320.577 Muscular Dystrophies 141
C16.320.728 Osteochondrodysplasias 125
C16.320.784 Pelger-Huet Anomaly 7
C16.320.812 Pycnodysostosis 2
C16.320.925 Werner Syndrome 14
C19.874 Thyroid Diseases 1 310
C19.874.410 Hyperthyroxinemia 5

Dysalbuminemic Hyperthyroxinemia Disease MeSH Browser