Human Phenotype Ontology 
Grandparent Node:
expandRetinal dystrophy (HP:0000556)help
Parent Node:
expandRod-cone dystrophy (HP:0000510)help
..Starting node
..expandPericentral retinitis pigmentosa (HP:0007947)help
Term ID: 7947
Name: Pericentral retinitis pigmentosa
Synonym:
Definition: A subtype of retinitis pigmentosa in which, instead of the pathology starting in the mid-periphery like typical retinitis pigmentosa, the disease starts in the near periphery closer to the vascular arcades and tends to spare the far periphery.
Comments:
Reference: HP:0007947
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandSectoral retinitis pigmentosa (HP:0031172) 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:0007947HP:0007947Pericentral retinitis pigmentosa0 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.