Human Gene Set: HP_ABNORMAL_FUNDUS_AUTOFLUORESCENCE_IMAGING


Standard name HP_ABNORMAL_FUNDUS_AUTOFLUORESCENCE_IMAGING
Systematic name M38391
Brief description Abnormal fundus autofluorescence imaging
Full description or abstract Fundus autofluorescence (FAF) is a non-invasive retinal imaging modality used in clinical practice to provide a density map of lipofuscin, the predominant ocular fluorophore, in the retinal pigment epithelium. Autofluorescent patterns result from the complex interaction of fluorophores such a lipofuscin, which release an autofluorescent signal, and elements such as melanin and rhodopsin, which absorb the excitation beam and attenuate autofluorescence. Other structures such as retinal vessels and the crystalline lens may also influence autofluorescence through blocking and interference. [PMID:27847630]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0030602
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0030602
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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 2023.1.Hs: Updated to HPO Release 2023-01-27.

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