Human Phenotype Ontology 
Grandparent Node:
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Abnormal lens morphology (HP:0000517)help
Parent Node:
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Ectopia lentis (HP:0001083)help
..Starting node
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Lens luxation (HP:0012019)help
Term ID: 12019
Name: Lens luxation
Synonym: Dislocated lens; Dislocated lenses
Definition: Complete dislocation of the lens of the eye.
Comments:
Reference: HP:0012019
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLens subluxation (HP:0001132) 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:0012019HP:0012019Lens luxation0C12ORF57 CL E G H11324629521OMIM:218340Temtamy syndrome.13
HP:0012019HP:0012019Lens luxation0COL11A1 CL E G H13012186OMIM:154780Marshall syndrome.215
HP:0012019HP:0012019Lens luxation0COL2A1 CL E G H12802200ORPHA:485Kniest dysplasiaHP:0040283 - Occasional284
HP:0012019HP:0012019Lens luxation0FBN1 CL E G H22003603OMIM:608328Weill-Marchesani syndrome 2, dominant1361
HP:0012019HP:0012019Lens luxation0MOCS1 CL E G H43377190OMIM:252150Molybdenum cofactor deficiency, complementation group A.96
HP:0012019HP:0012019Lens luxation0MOCS2 CL E G H43387193OMIM:252160Molybdenum cofactor deficiency, complementation group B.26
HP:0012019HP:0012019Lens luxation0PAX2 CL E G H50768616OMIM:120330Papillorenal syndromeHP:0040283 - Occasional39


Genes (7) :C12ORF57 COL11A1 COL2A1 FBN1 MOCS1 MOCS2 PAX2

Diseases (7) :OMIM:218340 OMIM:154780 ORPHA:485 OMIM:608328 OMIM:252150 OMIM:252160 OMIM:120330
 

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