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Hyperthyroxinemia, Familial Dysalbuminemic MeSH Descriptor Data 2022


MeSH Heading
Hyperthyroxinemia, Familial Dysalbuminemic
Tree Number(s)
C16.320.427
C19.874.410.249
Unique ID
D050010
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D050010
Scope Note
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.
Entry Term(s)
Familial Dysalbuminemic Hyperthyroxinemia
Previous Indexing
Serum Albumin (1982-2005)
Thyroxine (1982-2005)
Public MeSH Note
2006
History Note
2006
Date Established
2006/01/01
Date of Entry
2005/06/30
Revision Date
2005/08/02
Hyperthyroxinemia, Familial Dysalbuminemic Preferred
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