hyperthyroxinemia, familial dysalbuminemic

Preferred Label : hyperthyroxinemia, familial dysalbuminemic;

MeSH 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.;

MeSH synonym : familial dysalbuminemic hyperthyroxinemia; dysalbuminemic hyperthyroxinemia, familial;

Wikipedia link : https://en.wikipedia.org/wiki/Hyperthyroxinemia, familial dysalbuminemic;

Details

Origin ID

D050010;

UMLS CUI

C0342185;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- Familial Dysalbuminemic Hyperthyroidism [NCIt concept]
- Familial dysalbuminemic hyperthyroxinemia [PASCAL descriptor]
- Familial dysalbuminemic hyperthyroxinemia [ORDO Disease]
- Familial dysalbuminemic hyperthyroxinemia (disorder) [SNOMED CT concept]
- Hyperthyroxinemia, familial dysalbuminemic [OMIM Phenotype]
- familial dysalbuminaemic hyperthyroxinaemia [Disease (Nov.)]
Record concept(s)
- hyperthyroxinemia, familial dysalbuminemic [MeSH concept]
Related MeSH Supplementary Concept(s)
- dysalbuminemic hyperthyroxinemia [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Analbuminemia [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Dysalbuminemic Hyperthyroidism [NCIt concept]
- Familial dysalbuminemic hyperthyroxinemia [ORDO Disease]
- Familial dysalbuminemic hyperthyroxinemia [PASCAL descriptor]
- Familial dysalbuminemic hyperthyroxinemia (disorder) [SNOMED CT concept]
- Hyperthyroxinemia, familial dysalbuminemic [OMIM Phenotype]
- familial dysalbuminaemic hyperthyroxinaemia [Disease (Nov.)]

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