Human Phenotype Ontology 
Grandparent Node:
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Abnormal head blood vessel morphology (HP:3000036)help
Grandparent Node:
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Abnormal retinal vascular morphology (HP:0008046)help
Grandparent Node:
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Abnormal systemic arterial morphology (HP:0011004)help
Parent Node:
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Abnormal retinal artery morphology (HP:0000630)help
..Starting node
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Retinal arterial macroaneurysms (HP:0025355)help
Term ID: 25355
Name: Retinal arterial macroaneurysms
Synonym:
Definition: Acquired focal dilatations of branches of the retinal artery, usually second-order retinal arterioles, that range in size from 100 to 200 micrometers in diameter. Macroaneurysms are generally located at the termporal retina and may be hemorrhagic or exudative.
Comments:
Reference: HP:0025355
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCentral fundal arteriolar microaneurysms (HP:0008014) help
..expandCherry red spot of the macula (HP:0010729) help
..expandRetinal arterial occlusion (HP:0025326) help
..expandRetinal arterial tortuosity (HP:0000631) help
..expandRetinal arteriolar constriction (HP:0008043) help
..expandRetinal arteriolar occlusion (HP:0007985) help
..expandRetinal arteriolar tortuosity (HP:0001136) help
..expandRetinal arteritis (HP:0008030) 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:0025355HP:0025355Retinal arterial macroaneurysms0IGFBP7 CL E G H34905476OMIM:614224Retinal arterial macroaneurysm with supravalvular pulmonic stenosis.2


Genes (1) :IGFBP7

Diseases (1) :OMIM:614224
 

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