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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Corneolenticular adhesion (HP:0011485)help
Term ID: 11485
Name: Corneolenticular adhesion
Synonym:
Definition: Developmental abnormality in which the lens and cornea are not separated.
Comments:
Reference: HP:0011485
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
..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:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011485HP:0011485Corneolenticular adhesion0 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.