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Digital medicine Outcomes Value Set (DOVeS) Ontology
| Preferred Name | hyperthyroxinemia, familial dysalbuminemic | |
| Synonyms |
euthyroid hyperthyroxinemia 1 FDH FDAH hyperthyroxinemia, familial Dysalbuminemic hyperthyroxinemia, familial dysalbuminemic dysalbuminemic hyperthyroxinemia dysalbuminemic hypertriiodothyroninemia familial Dysalbuminemic hyperthyroxinemia bisalbuminemia familial Dysalbuminemic hyperthyroidism |
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| Definitions |
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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| ID |
http://purl.obolibrary.org/obo/MONDO_0014448 |
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| altLabel |
euthyroid hyperthyroxinemia 1 FDH FDAH hyperthyroxinemia, familial Dysalbuminemic hyperthyroxinemia, familial dysalbuminemic dysalbuminemic hyperthyroxinemia dysalbuminemic hypertriiodothyroninemia familial Dysalbuminemic hyperthyroxinemia bisalbuminemia familial Dysalbuminemic hyperthyroidism
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| 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.
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| has_exact_synonym |
hyperthyroxinemia, familial Dysalbuminemic hyperthyroxinemia, familial dysalbuminemic dysalbuminemic hyperthyroxinemia dysalbuminemic hypertriiodothyroninemia familial Dysalbuminemic hyperthyroxinemia bisalbuminemia familial Dysalbuminemic hyperthyroidism
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| has_related_synonym |
euthyroid hyperthyroxinemia 1 FDH FDAH
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| IAO_0000233 | ||
| label |
hyperthyroxinemia, familial dysalbuminemic
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| prefixIRI |
MONDO:0014448
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| prefLabel |
hyperthyroxinemia, familial dysalbuminemic
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| textual 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.
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| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0005333 |
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