Human Phenotype Ontology 
Grandparent Node:
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Abnormal fundus autofluorescence imaging (HP:0030602)help
Parent Node:
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Perifoveal ring of hyperautofluorescence (HP:0030629)help
..Starting node
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Perifoveal ring of hyperautofluorescence surrounded by normal autofluorescence (HP:0030633)help
Term ID: 30633
Name: Perifoveal ring of hyperautofluorescence surrounded by normal autofluorescence
Synonym:
Definition:
Comments:
Reference: HP:0030633
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPerifoveal ring of hyperautofluorescence surrounded by abnormal autofluorescence (HP:0030634) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030633HP:0030633Perifoveal ring of hyperautofluorescence surrounded by normal autofluorescence0 CL E G H


Genes (0) :

Diseases (0) :
 

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