Human Phenotype Ontology 
Grandparent Node:
expandAbnormal fundus morphology (HP:0001098)help
Parent Node:
expandAbnormality of the optic nerve (HP:0000587)help
..Starting node
..expandOptic nerve arteriovenous malformation (HP:0031256)help
Term ID: 31256
Name: Optic nerve arteriovenous malformation
Synonym:
Definition: An arteriovenous malformation is a disruption of the normal vascular pattern in which arteries or arterioles connect directly to the venous collection system, bypassing any capillary bed. This term refers to an arteriovenous malformation located in the optic nerve.
Comments:
Reference: HP:0031256
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal optic disc morphology (HP:0012795) help
..expandAbnormality of optic chiasm morphology (HP:0025163) help
..expandAplasia/Hypoplasia of the optic nerve (HP:0008058) help
..expandLeber optic atrophy (HP:0001112) help
..expandMarcus Gunn pupil (HP:0200057) help
..expandMorning glory anomaly (HP:0025514) help
..expandOptic disc coloboma (HP:0000588) help
..expandOptic nerve compression (HP:0007807) help
..expandOptic nerve dysplasia (HP:0001093) help
..expandOptic nerve misrouting (HP:0025551) help
..expandOptic neuritis (HP:0100653) help
..expandOptic neuropathy (HP:0001138) 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:0031256HP:0031256Optic nerve arteriovenous malformation0 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.