Human Gene Set: HP_HYPOPIGMENTATION_OF_THE_FUNDUS


Standard name HP_HYPOPIGMENTATION_OF_THE_FUNDUS
Systematic name M37142
Brief description Hypopigmentation of the fundus
Full description or abstract Reduced pigmentation of the fundus, typically generalized. Fundoscopy may reveal a low level pigment in both RPE and choroid with clear visibility of choroidal vessels (pale/albinoid) or low pigment level in the RPE with deep pigment in choroid so that visible choroidal vessels are separated by deeply pigmented zones (tesselated/tigroid). [https://orcid.org/0000-0003-0986-4123]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007894
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007894
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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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