Human Gene Set: HP_OSTEOCHONDROSIS


Standard name HP_OSTEOCHONDROSIS
Systematic name M38601
Brief description Osteochondrosis
Full description or abstract Abnormal growth ossification centers in children. Initially a degeneration/ necrosis followed by regeneration or recalcification. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0040188
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0040188
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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 12 genes
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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