Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Grandparent Node:
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Fundus hemorrhage (HP:0031803)help
Grandparent Node:
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Hemorrhage of the eye (HP:0011885)help
Parent Node:
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Retinal hemorrhage (HP:0000573)help
..Starting node
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Subretinal hemorrhage (HP:0025243)help
Term ID: 25243
Name: Subretinal hemorrhage
Synonym: Subretinal haemorrhage; Subretinal heme
Definition: Accumulation of blood located beneath the neurosensory retina in the space between the neurosensory retina and the retinal pigment epithelium.
Comments:
Reference: HP:0025243
Genes and Diseases:
 
       Child Nodes:
........expandSubmacular hemorrhage (HP:0025582) help

 Sister Nodes: 
..expandIntraretinal hemorrhage (HP:0031805) help
..expandMacular hemorrhage (HP:0025574) help
..expandSub-inner limiting membrane hemorrhage (HP:0031611) help
..expandSubretinal pigment epithelium hemorrhage (HP:0025244) 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:0025243HP:0025243Subretinal hemorrhage0 CL E G H
HP:0025243HP:0025582Submacular hemorrhage1 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.