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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Vitritis (HP:0011531)help
Term ID: 11531
Name: Vitritis
Synonym: Hyalitis; Vitreitis
Definition: Inflammation of the vitreous body, characterized by the presence of inflammatory cells and protein exudate in the vitreous cavity.
Comments:
Reference: HP:0011531
Genes and Diseases:
 
       Child Nodes:
........expandVitreous haze (HP:0030652) help
........expandVitreous snowballs (HP:0030661) help
........expandVitreous inflammatory cells (HP:0030662) help

 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
..expandOptically empty vitreous (HP:0030663) 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
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011531HP:0011531Vitritis0COX7B CL E G H13492291ORPHA:2556Microphthalmia with linear skin defects syndromeHP:0040282 - Frequent6
HP:0011531HP:0011531Vitritis0HCCS CL E G H30524837ORPHA:2556Microphthalmia with linear skin defects syndromeHP:0040282 - Frequent11
HP:0011531HP:0011531Vitritis0HLA-A CL E G H31054931ORPHA:179Birdshot chorioretinopathyHP:0040281 - Very frequent4
HP:0011531HP:0011531Vitritis0NDUFB11 CL E G H5453920372ORPHA:2556Microphthalmia with linear skin defects syndromeHP:0040282 - Frequent3
HP:0011531HP:0011531Vitritis0RB1 CL E G H59259884OMIM:180200RETINOBLASTOMAHP:0040283 - Occasional365
HP:0011531HP:0030652Vitreous haze1 CL E G H
HP:0011531HP:0030662Vitreous inflammatory cells1 CL E G H
HP:0011531HP:0030661Vitreous snowballs1 CL E G H


Genes (5) :COX7B HCCS HLA-A NDUFB11 RB1

Diseases (3) :ORPHA:2556 ORPHA:179 OMIM:180200
 

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