Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vascular morphology (HP:0025015)help
Parent Node:
expandAbnormal retinal artery morphology (HP:0000630)help
Parent Node:
expandVascular dilatation (HP:0002617)help
..Starting node
..expandCentral fundal arteriolar microaneurysms (HP:0008014)help
Term ID: 8014
Name: Central fundal arteriolar microaneurysms
Synonym:
Definition: Microscopic aneurysms of the retinal arterioles near the central part of the fundus, visible as small round dark red dots on the retinal surface (not arising from visible vessels) that are by definition less than the diameter of the major optic veins as they cross the optic disc.
Comments:
Reference: HP:0008014
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAortic aneurysm (HP:0004942) help
..expandDilatation of an abdominal artery (HP:0002636) help
..expandDilatation of the cerebral artery (HP:0004944) help
..expandDilatation of the ductus arteriosus (HP:0030745) help
..expandDilatation of the ventricular cavity (HP:0006698) help
..expandPseudoaneurysm (HP:0031625) 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:0008014HP:0008014Central fundal arteriolar microaneurysms0 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.