Human Phenotype Ontology 
Grandparent Node:
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Abnormal posterior eye segment morphology (HP:0004329)help
Parent Node:
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Abnormal vitreous humor morphology (HP:0004327)help
..Starting node
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Optically empty vitreous (HP:0030663)help
Term ID: 30663
Name: Optically empty vitreous
Synonym:
Definition: Vestigial vitreous gel occupying the immediate retrolental space and minimal to no discernable gel in the central vitreous cavity, giving the appearance of an empty vitreous cavity.
Comments:
Reference: HP:0030663
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAmyloid deposition in the vitreous humor (HP:0007841) help
..expandAsteroid hyalosis (HP:0030672) help
..expandBeaded vitreous appearance (HP:0031154) help
..expandMembranous vitreous appearance (HP:0031153) help
..expandPeripheral vitreous opacities (HP:0007710) help
..expandPosterior vitreous detachment (HP:0001489) help
..expandRemnants of the hyaloid vascular system (HP:0007968) help
..expandVitreoretinopathy (HP:0007773) help
..expandVitreous floaters (HP:0100832) help
..expandVitreous hemorrhage (HP:0007902) help
..expandVitritis (HP:0011531) 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:0030663HP:0030663Optically empty vitreous0COL2A1 CL E G H12802200OMIM:609508STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR284
HP:0030663HP:0030663Optically empty vitreous0KCNJ13 CL E G H37696259OMIM:193230Snowflake vitreoretinal degenerationHP:0040283 - Occasional42
HP:0030663HP:0030663Optically empty vitreous0VCAN CL E G H14622464OMIM:143200Wagner vitreoretinopathy180


Genes (3) :COL2A1 KCNJ13 VCAN

Diseases (3) :OMIM:609508 OMIM:193230 OMIM:143200
 

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