Link to this page
Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/D050010
http://purl.bioontology.org/ontology/MESH/D050010
|
|---|---|
| Preferred Name | Hyperthyroxinemia, Familial Dysalbuminemic |
| 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.
|
| Synonyms |
Familial Dysalbuminemic Hyperthyroxinemia
Dysalbuminemic Hyperthyroxinemia, Familial
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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. |
|---|---|
| altLabel |
Familial Dysalbuminemic Hyperthyroxinemia
Dysalbuminemic Hyperthyroxinemia, Familial
|
| prefLabel | Hyperthyroxinemia, Familial Dysalbuminemic
|
| Machine permutation | 2006
|
| HN | 2006
|
| Mapped from | |
| type | |
| tui | T047
|
| TERMUI |
T607700
T607699
|
| TH | NLM (2006)
|
| MMR | 20060101
|
| notation | D050010
|
| Semantic type UMLS property | |
| Inverse of AQ |
See more
See less
|
| DX | 20060101
|
| cui | C0342185
|
| DC | 1
|
| MN |
C19.874.410.249
C16.320.427
|
| AQL | BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
|
| MDA | 20040902
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |