Human Gene Set: HP_HYPERTHYROIDISM


Standard name HP_HYPERTHYROIDISM
Systematic name M34967
Brief description Hyperthyroidism
Full description or abstract An abnormality of thyroid physiology characterized by excessive secretion of the thyroid hormones thyroxine (i.e., T4) and/or 3,3',5-triiodo-L-thyronine zwitterion (i.e., triiodothyronine or T3). [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000836
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000836
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 37 genes
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Show members (show 37 source identifiers mapped to 37 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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