Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Grandparent Node:
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Abnormality of the vasculature of the eye (HP:0008047)help
Parent Node:
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Abnormal retinal vascular morphology (HP:0008046)help
..Starting node
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Increased retinal vascularity (HP:0007986)help
Term ID: 7986
Name: Increased retinal vascularity
Synonym:
Definition:
Comments:
Reference: HP:0007986
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal distribution of retinal arterioles and venules (HP:0007815) help
..expandAbnormal retinal artery morphology (HP:0000630) help
..expandAttenuation of retinal blood vessels (HP:0007843) help
..expandHypertensive retinopathy (HP:0001095) help
..expandLipemia retinalis (HP:0000660) help
..expandPeripheral retinal avascularization (HP:0007685) help
..expandRetinal neovascularization (HP:0030666) help
..expandRetinal telangiectasia (HP:0007763) help
..expandRetinal vascular malformation (HP:0007797) help
..expandRetinal vascular proliferation (HP:0007850) help
..expandRetinal vascular tortuosity (HP:0012841) help
..expandRetinal vasculitis (HP:0025188) help
..expandRetinal vein occlusion (HP:0012636) 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:0007986HP:0007986Increased retinal vascularity0 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.