Human Phenotype Ontology 
Grandparent Node:
expandAbnormal macular morphology (HP:0001103)help
Parent Node:
expandAbnormality morphology of the macular vasculature (HP:0030495)help
..Starting node
..expandMacular exudate (HP:0030496)help
Term ID: 30496
Name: Macular exudate
Synonym: Macular exudates; Macular exudation
Definition: Yellow-white intraretinal deposits in the macula typically associated with damaged outer blood-retina barrier and exudation of serous fluid and lipids from the retinal microvasculature.
Comments:
Reference: HP:0030496
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMacular microaneurysm/hemorrhage (HP:0030494) help
..expandMacular telangiectasia (HP:0030503) 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:0030496HP:0030496Macular exudate0CTNNB1 CL E G H14992514ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional88
HP:0030496HP:0030496Macular exudate0FZD4 CL E G H83224042ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional109
HP:0030496HP:0030496Macular exudate0LRP5 CL E G H40416697ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional125
HP:0030496HP:0030496Macular exudate0NDP CL E G H46937678ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0030496HP:0030496Macular exudate0TSPAN12 CL E G H2355421641ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional39
HP:0030496HP:0030496Macular exudate0ZNF408 CL E G H7979720041ORPHA:891Familial exudative vitreoretinopathyHP:0040283 - Occasional14


Genes (6) :CTNNB1 FZD4 LRP5 NDP TSPAN12 ZNF408

Diseases (1) :ORPHA:891
 

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