Human Gene Set: HP_PITUITARY_HYPOTHYROIDISM


Standard name HP_PITUITARY_HYPOTHYROIDISM
Systematic name M41358
Brief description Pituitary hypothyroidism
Full description or abstract A type of hypothyroidism that results from a defect in thyroid-stimulating hormone secretion. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0008245
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0008245
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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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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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