Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the thyroid gland (HP:0000820)help
Parent Node:
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Abnormality of thyroid physiology (HP:0002926)help
..Starting node
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Euthyroid hyperthyroxinemia (HP:0008247)help
Term ID: 8247
Name: Euthyroid hyperthyroxinemia
Synonym: Asymptomatic hyperthyroxinemia
Definition: An abnormality of thyroid physiology (HP:0002926) characterized by increased levels of thyroxine without evidence of clinical thyroid disease.
Comments:
Reference: HP:0008247
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal circulating thyroid hormone concentration (HP:0031508) help
..expandAbnormal radioactive iodine uptake test result (HP:0031221) help
..expandHyperthyroidism (HP:0000836) help
..expandHypothyroidism (HP:0000821) help
..expandImpaired sensitivity to thyroid hormone (HP:0002930) help
..expandImpaired sensitivity to thyroid stimulating hormone (HP:0011789) help
..expandPositive perchlorate discharge test (HP:0025482) help
..expandThyroid defect in oxidation and organification of iodide (HP:0008263) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008247HP:0008247Euthyroid hyperthyroxinemia0CDH23 CL E G H6407213733ORPHA:91347TSH-secreting pituitary adenomaHP:0040283 - Occasional636


Genes (1) :CDH23

Diseases (1) :ORPHA:91347
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.