Human Gene Set: HP_OSTEOPOROSIS


Standard name HP_OSTEOPOROSIS
Systematic name M35029
Brief description Osteoporosis
Full description or abstract Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility. According to the WHO criteria, osteoporosis is defined as a BMD that lies 2.5 standard deviations or more below the average value for young healthy adults (a T-score below -2.5 SD). [https://orcid.org/0000-0002-0736-9199, PMID:28293453]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000939
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000939
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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
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NCI-60 cell lines (National Cancer Institute)

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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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