Human Gene Set: HP_ABNORMALITY_OF_RETINAL_PIGMENTATION


Standard name HP_ABNORMALITY_OF_RETINAL_PIGMENTATION
Systematic name M37117
Brief description Abnormality of retinal pigmentation
Full description or abstract  
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007703
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007703
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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)
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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