Human Phenotype Ontology 
Grandparent Node:
Abnormal pupillary function (HP:0007686)help
Parent Node:
Mydriasis (HP:0011499)help
..Starting node
Bilateral congenital mydriasis (HP:0007932)help
Term ID: 7932
Name: Bilateral congenital mydriasis
Definition: Congenital abnormal dilation of the pupil on both sides.
Reference: HP:0007932
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:0007932HP:0007932Bilateral congenital mydriasis0 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 June 2019 release.