Human Phenotype Ontology 
Grandparent Node:
expandAbnormal posterior eye segment morphology (HP:0004329)help
Parent Node:
expandAbnormal vitreous humor morphology (HP:0004327)help
..Starting node
..expandAmyloid deposition in the vitreous humor (HP:0007841)help
Term ID: 7841
Name: Amyloid deposition in the vitreous humor
Synonym: Amyloid deposition in the vitreous humour; Vitreous amyloid deposits
Definition: Deposition of hyaline extracellular material (amyloid) into the vitreous humor, which can manifest as vitreous opacities and reduced visual acuity.
Comments:
Reference: HP:0007841
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..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
..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:0007841HP:0007841Amyloid deposition in the vitreous humor0TTR CL E G H727612405OMIM:105210Amyloidosis, hereditary, transthyretin-related.107


Genes (1) :TTR

Diseases (1) :OMIM:105210
 

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