Human Phenotype Ontology 
Grandparent Node:
expandRetinal degeneration (HP:0000546)help
Parent Node:
expandPeripheral retinal degeneration (HP:0007769)help
..Starting node
..expandPeripheral cystoid retinal degeneration (HP:0007667)help
Term ID: 7667
Name: Peripheral cystoid retinal degeneration
Synonym: Cystic retinal degeneration; Peripheral cystoid degeneration
Definition: Degenerative changes of the peripheral retina consisting of close-packed tiny cystic spaces at the outer plexiform/inner nuclear retinal level. The degeneration is very common in adult eyes and starts adjacent to the ora serrata and extends circumferentially and posteriorly.
Comments:
Reference: HP:0007667
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLattice retinal degeneration (HP:0007992) help
..expandobsolete Peripheral retinal cone degeneration (HP:0007782) help
..expandReticular pigmentary degeneration (HP:0007937) help
..expandSnowflake vitreoretinal degeneration (HP:0011533) 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:0007667HP:0007667Peripheral cystoid retinal degeneration0RS1 CL E G H624710457OMIM:312700Retinoschisis 1, X-linked, juvenile.148


Genes (1) :RS1

Diseases (1) :OMIM:312700
 

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