Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Abnormal vitreous humor morphology (HP:0004327)help
Parent Node:
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Abnormality of vision (HP:0000504)help
..Starting node
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Vitreous floaters (HP:0100832)help
Term ID: 100832
Name: Vitreous floaters
Synonym: Eye floaters; Flitting flies; Mouches volantes; Myodeopsia; Myodesopsia; Spots in front of eyes; Vitreous condensations; Vitreous debris; Vitreous opacities; Vitreous veils
Definition: Deposits of various size, shape, consistency, refractive index, and motility within the eye's vitreous humour, which is normally transparent.
Comments:
Reference: HP:0100832
Genes and Diseases:
 
       Child Nodes:
........expandVitreous strands (HP:0030832) help

 Sister Nodes: 
..expandAbnormality of binocular vision (HP:0011514) help
..expandAmaurosis fugax (HP:0100576) help
..expandBlurred vision (HP:0000622) help
..expandBradyopsia (HP:0030511) help
..expandColor vision defect (HP:0000551) help
..expandDifficulty adjusting to changes in luminance (HP:0030512) help
..expandHemeralopia (HP:0012047) help
..expandMetamorphopsia (HP:0012508) help
..expandNyctalopia (HP:0000662) help
..expandPhotophobia (HP:0000613) help
..expandPhotopsia (HP:0030786) help
..expandPoor visual behavior for age (HP:0025152) help
..expandReduced visual acuity (HP:0007663) help
..expandVisual field defect (HP:0001123) help
..expandVisual impairment (HP:0000505) help
..expandVisual loss (HP:0000572) 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:0100832HP:0100832Vitreous floaters0ARL3 CL E G H403694OMIM:618173RETINITIS PIGMENTOSA 83; RP831
HP:0100832HP:0100832Vitreous floaters0ARSK CL E G H15364225239OMIM:619698MUCOPOLYSACCHARIDOSIS, TYPE X; MPS10
HP:0100832HP:0100832Vitreous floaters0CTNNB1 CL E G H14992514ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional88
HP:0100832HP:0100832Vitreous floaters0FZD4 CL E G H83224042OMIM:133780Exudative vitreoretinopathy 1109
HP:0100832HP:0100832Vitreous floaters0FZD4 CL E G H83224042ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional109
HP:0100832HP:0100832Vitreous floaters0HLA-A CL E G H31054931ORPHA:179Birdshot chorioretinopathyHP:0040282 - Frequent4
HP:0100832HP:0100832Vitreous floaters0LRP5 CL E G H40416697OMIM:133780Exudative vitreoretinopathy 1125
HP:0100832HP:0100832Vitreous floaters0LRP5 CL E G H40416697ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional125
HP:0100832HP:0100832Vitreous floaters0NDP CL E G H46937678ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0100832HP:0100832Vitreous floaters0P3H2 CL E G H5521419317OMIM:614292Myopia, high, with cataract and vitreoretinal degeneration5
HP:0100832HP:0100832Vitreous floaters0PAK2 CL E G H50628591OMIM:618458
HP:0100832HP:0100832Vitreous floaters0TSPAN12 CL E G H2355421641ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0100832HP:0100832Vitreous floaters0TTR CL E G H727612405ORPHA:85447ATTRV30M amyloidosisHP:0040282 - Frequent107
HP:0100832HP:0100832Vitreous floaters0ZNF408 CL E G H7979720041ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional14
HP:0100832HP:0030832Vitreous strands1 CL E G H


Genes (12) :ARL3 ARSK CTNNB1 FZD4 HLA-A LRP5 NDP P3H2 PAK2 TSPAN12 TTR ZNF408

Diseases (8) :OMIM:618173 OMIM:619698 ORPHA:891 OMIM:133780 ORPHA:179 OMIM:614292 OMIM:618458 ORPHA:85447
 

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