Human Phenotype Ontology 
Grandparent Node:
Abnormality of the orbital region (HP:0000315)help
Parent Node:
Aplasia/Hypoplasia of the lens (HP:0008063)help
Parent Node:
Coloboma (HP:0000589)help
..Starting node
Lens coloboma (HP:0100719)help
Term ID: 100719
Name: Lens coloboma
Definition: A sectoral indentation of the crystalline lens, usually due to zonular weakness or absence.
Reference: HP:0100719
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandChorioretinal coloboma (HP:0000567) help
..expandCiliary body coloboma (HP:0020006) help
..expandIris coloboma (HP:0000612) help
..expandOptic nerve coloboma (HP:0000588) help
..expandRetinal coloboma (HP:0000480) help
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:0100719HP:0100719Lens coloboma0FGF3 CL E G H22482791ORPHA020353681164950

Genes (1) :FGF3

Diseases (1) :2791

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.