Human Phenotype Ontology 
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obsolete Pericentral pigmentary retinopathy (HP:0007852)help
Term ID: 7852
Name: obsolete Pericentral pigmentary retinopathy
Synonym:
Definition:
Comments:
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.