Human Gene Set: HP_GEOGRAPHIC_ATROPHY


Standard name HP_GEOGRAPHIC_ATROPHY
Systematic name M38491
Brief description Geographic atrophy
Full description or abstract Sharply demarcated area of partial or complete depigmentation of the fundus reflecting atrophy of the retinal pigment epithelium with associated retinal photoreceptor loss. The margins of the de-pigmented area are usually scalloped and the large choroidal vessels are visible through the atrophic retinal pigment epithelium. [https://orcid.org/0000-0003-0986-4123, PMID:24158023]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0031609
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0031609
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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
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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