Human Gene Set: HP_RETINAL_ATROPHY


Standard name HP_RETINAL_ATROPHY
Systematic name M35130
Brief description Retinal atrophy
Full description or abstract Well-demarcated area(s) of partial or complete depigmentation in the fundus, reflecting atrophy of the retinal pigment epithelium with associated retinal photoreceptor loss. [https://orcid.org/0000-0003-0986-4123]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0001105
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0001105
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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 2025.1.Hs: Updated to HPO Release 2025-05-06.

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