Human Phenotype Ontology 
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Perifoveal hypoautofluorescence (HP:0034272)help
Term ID: 34272
Name: Perifoveal hypoautofluorescence
Synonym:
Definition: Decreased amount of autofluorescence (emission of fluorescent light from ocular structures in the absence of sodium fluorescein) in the retina in the region surrounding the fovea.
Comments:
Reference: HP:0034272
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0034272HP:0034272Perifoveal hypoautofluorescence0RPGR CL E G H610310295OMIM:300029Retinitis pigmentosa 3200


Genes (1) :RPGR

Diseases (1) :OMIM:300029
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.