Human Phenotype Ontology 
Grandparent Node:
Abnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
Abnormal anterior chamber morphology (HP:0000593)help
..Starting node
Absent anterior chamber of the eye (HP:0008037)help
Term ID: 8037
Name: Absent anterior chamber of the eye
Definition: Absence of the anterior chamber of the eye owing to a developmental defect.
Reference: HP:0008037
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal trabecular meshwork morphology (HP:0012630) help
..expandAnterior chamber cells (HP:0025560) help
..expandAnterior chamber cyst (HP:0025311) help
..expandAnterior chamber flare (HP:0031616) help
..expandAnterior chamber inflammatory cells (HP:0031701) help
..expandAnterior chamber red blood cells (HP:0031702) help
..expandAnterior chamber synechiae (HP:0007833) help
..expandCorneolenticular adhesion (HP:0011485) help
..expandDeep anterior chamber (HP:0007765) help
..expandHypopyon (HP:0031615) help
..expandOcular anterior segment dysgenesis (HP:0007700) help
..expandShallow anterior chamber (HP:0000594) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0008037HP:0008037Absent anterior chamber of the eye0LRP5 CL E G H4041259770Osteoporosis with pseudoglioma259770C0432252OMIM12214116697603506
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :LRP5

Diseases (1) :259770

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