Human Phenotype Ontology 
..Starting node
obsolete Pericentral pigmentary retinopathy (HP:0007852)help
Term ID: 7852
Name: obsolete Pericentral pigmentary retinopathy
Reference: HP:0007852
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007852HP:0007852obsolete Pericentral pigmentary retinopathy0 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 August 2021 release.