Human Phenotype Ontology 
Grandparent Node:
obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
Abnormal anterior eye segment morphology (HP:0004328)help
..Starting node
Abnormal suspensory ligament of lens morphology (HP:0012628)help
Term ID: 12628
Name: Abnormal suspensory ligament of lens morphology
Synonym: Abnormality of the suspensory ligament of lens; Abnormality of zinn's membrane; Ciliary zonule abnormality; Zonule of zinn abnormality
Definition: An anomaly of the suspensory ligament of lens, also known as the ciliary zonule. These ligaments represent a series of fibers connecting the ciliary body and lens of the eye, holding the lens in place.
Reference: HP:0012628
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormal anterior chamber morphology (HP:0000593) help
..expandAbnormal cornea morphology (HP:0000481) help
..expandAbnormal lens morphology (HP:0000517) help
..expandAbnormality iris morphology (HP:0000525) help
..expandAplasia/Hypoplasia affecting the anterior segment of the eye (HP:0008062) help
..expandPseudoexfoliation (HP:0012627) 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:0012628HP:0012628Abnormal suspensory ligament of lens morphology0C1QTNF5 CL E G H11490214344ORPHA:67042Late-onset retinal degenerationHP:0040283 - Occasional20

Genes (1) :C1QTNF5

Diseases (1) :ORPHA:67042

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