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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0100832HP:0100832Vitreous floaters0ARL3 CL E G H403618173RETINITIS PIGMENTOSA 83618173OMIM1363694604695
HP:0100832HP:0100832Vitreous floaters0HLA-A CL E G H3105179Macrothrombocytopenia progressive deafnessORPHA177184931142800
HP:0100832HP:0100832Vitreous floaters0TTR CL E G H727685447ORPHA115128012405176300
HP:0100832HP:0100832Vitreous floaters1ARL3 CL E G H403618173RETINITIS PIGMENTOSA 83618173OMIM1363694604695
HP:0100832HP:0100832Vitreous floaters1HLA-A CL E G H3105179Macrothrombocytopenia progressive deafnessORPHA177184931142800
HP:0100832HP:0100832Vitreous floaters1TTR CL E G H727685447ORPHA115128012405176300
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (3) :ARL3 HLA-A TTR

Diseases (3) :618173 179 85447
 

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