Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
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Abnormal anterior chamber morphology (HP:0000593)help
..Starting node
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Deep anterior chamber (HP:0007765)help
Term ID: 7765
Name: Deep anterior chamber
Synonym:
Definition: Increased depth of the anterior chamber, i.e., the anteroposterior distance between the cornea and the iris is increased.
Comments:
Reference: HP:0007765
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal trabecular meshwork morphology (HP:0012630) help
..expandAbsent anterior chamber of the eye (HP:0008037) 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
..expandHypopyon (HP:0031615) help
..expandOcular anterior segment dysgenesis (HP:0007700) help
..expandShallow anterior chamber (HP:0000594) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007765HP:0007765Deep anterior chamber0CHRDL1 CL E G H9185129861OMIM:309300MEGALOCORNEA9
HP:0007765HP:0007765Deep anterior chamber0LTBP2 CL E G H40536715OMIM:251750Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucomaHP:0040283 - Occasional123


Genes (2) :CHRDL1 LTBP2

Diseases (2) :OMIM:309300 OMIM:251750
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.