Familial dysalbuminemic hyperthyroxinemia
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| Familial dysalbuminemic hyperthyroxinemia | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 103600 |
| DiseasesDB | 32942 |
| Patient UK | Familial dysalbuminemic hyperthyroxinemia |
| MeSH | D050010 |
Familial dysalbuminemic hyperthyroxinemia is a type of hyperthyroxinemia associated with mutations in the human serum albumin gene.[1]
The term was introduced in 1982.[2]
References
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This article about an endocrine, nutritional or metabolic disease is a stub. You can help Wikipedia by expanding it. |
