Descriptor English: | Hyperthyroxinemia, Familial Dysalbuminemic | ||||
Descriptor Spanish: |
Hipertiroxinemia Disalbuminémica Familiar
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Descriptor Portuguese: | Hipertireoxinemia Disalbuminêmica Familiar | ||||
Descriptor French: | Hyperthyroxinémie dysalbuminémique familiale | ||||
Entry term(s): |
Dysalbuminemic Hyperthyroxinemia, Familial Familial Dysalbuminemic Hyperthyroxinemia |
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Tree number(s): |
C16.320.427 C19.874.410.249 |
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RDF Unique Identifier: | https://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. |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Previous Indexing: |
Serum Albumin (1982-2005) Thyroxine (1982-2005) |
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Public MeSH Note: | 2006 |
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History Note: | 2006 |
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DeCS ID: | 50510 | ||||
Unique ID: | D050010 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 2006/01/01 | ||||
Date of Entry: | 2005/06/30 | ||||
Revision Date: | 2005/08/02 |
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Hyperthyroxinemia, Familial Dysalbuminemic
- Preferred
Concept UI |
M0471943 |
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. |
Preferred term | Hyperthyroxinemia, Familial Dysalbuminemic |
Entry term(s) |
Dysalbuminemic Hyperthyroxinemia, Familial Familial Dysalbuminemic Hyperthyroxinemia |
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