Human Gene Set: HP_ABNORMAL_TRANSFERRIN_SATURATION


Standard name HP_ABNORMAL_TRANSFERRIN_SATURATION
Systematic name M38588
Brief description Abnormal transferrin saturation
Full description or abstract Any abnormality in the serum transferrin saturation, which is calculated by dividing the serum iron level by total iron-binding capacity. [PMID:15083853]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0040135
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0040135
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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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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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