Human Gene Set: HP_HYPERAUTOFLUORESCENT_RETINAL_LESION


Standard name HP_HYPERAUTOFLUORESCENT_RETINAL_LESION
Systematic name M41484
Brief description Hyperautofluorescent retinal lesion
Full description or abstract Increased amount of autofluorescence in the retina as ascertained by fundus autofluorescence imaging. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0025158
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0025158
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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)
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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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