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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Sub-inner limiting membrane hemorrhage (HP:0031611)help
Term ID: 31611
Name: Sub-inner limiting membrane hemorrhage
Synonym: Sub-ILM haemorrhage; Sub-ILM hemorrhage; Sub-inner limiting membrane haemorrhage
Definition: A type of intraretinal hemorrhage that is located in the superficial retina between the inner limiting membrane and the retinal nerve fiber layer.
Comments:
Reference: HP:0031611
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandIntraretinal hemorrhage (HP:0031805) help
..expandMacular hemorrhage (HP:0025574) help
..expandSubretinal hemorrhage (HP:0025243) 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:0031611HP:0031611Sub-inner limiting membrane 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.