Human Phenotype Ontology 
Grandparent Node:
expandFundus hemorrhage (HP:0031803)help
Parent Node:
expandPreretinal hemorrhage (HP:0025240)help
..Starting node
..expandSubhyaloid hemorrhage (HP:0025239)help
Term ID: 25239
Name: Subhyaloid hemorrhage
Synonym: Subhyaloid haemorrhage; Subhyaloid heme
Definition: A localized detachment of the vitreous from the retina due to the accumulation of blood. When localized in the macular area, it results in sudden profound loss of vision. Subhyaloid premacular hemorrhage is typically characterized by a circumscribed, round or dumb-bell shaped, bright red mound of blood beneath the internal limiting membrane (ILM) or between the ILM and hyaloid face, in or near to the central macular area.
Comments:
Reference: HP:0025239
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPremacular hemorrhage (HP:0031804) 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:0025239HP:0025239Subhyaloid hemorrhage0 CL E G H


Genes (0) :

Diseases (0) :
 

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