Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior eye segment morphology (HP:0004328)help
Grandparent Node:
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Aplasia/Hypoplasia affecting the eye (HP:0008056)help
Parent Node:
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Abnormality of the lens (HP:0000517)help
Parent Node:
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Aplasia/Hypoplasia affecting the anterior segment of the eye (HP:0008062)help
..Starting node
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Aplasia/Hypoplasia of the lens (HP:0008063)help
Term ID: 8063
Name: Aplasia/Hypoplasia of the lens
Synonym: Absent/small lens; Absent/underdeveloped lens
Definition: Absence or underdevelopment of the lens.
Comments:
Reference: HP:0008063
Genes and Diseases:
 
       Child Nodes:
........expandAphakia (HP:0007707) help
................... HP:0500081 Pseudophakia
........expandMicrophakia (HP:0012376) help
........expandMicrospherophakia (HP:0030961) help
........expandLens coloboma (HP:0100719) help

 Sister Nodes: 
..expandAnterior segment of eye aplasia (HP:0007779) help
..expandAplasia/Hypoplasia of the iris (HP:0008053) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008063HP:0008063Aplasia/Hypoplasia of the lens0NDP CL E G H4693649ORPHA11672437678300658
HP:0008063HP:0008063Aplasia/Hypoplasia of the lens0XYLT2 CL E G H6413285194ORPHA1138315517608125
HP:0008063HP:0008063Aplasia/Hypoplasia of the lens1NDP CL E G H4693649ORPHA11672437678300658
HP:0008063HP:0008063Aplasia/Hypoplasia of the lens1XYLT2 CL E G H6413285194ORPHA1138315517608125
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (10) :ADAMTS10 CPAMD8 FBN1 FGF3 FOXE3 HMX1 LMX1B LTBP2 NDP XYLT2

Diseases (12) :649 85194 277600 617319 608328 2791 83461 610256 612109 161200 251750 614819
 

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