Human Phenotype Ontology 
Grandparent Node:
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Abnormal fundus morphology (HP:0001098)help
Parent Node:
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Abnormality of the optic nerve (HP:0000587)help
..Starting node
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Optic nerve dysplasia (HP:0001093)help
Term ID: 1093
Name: Optic nerve dysplasia
Synonym:
Definition: The presence of developmental dysplasia of the optic nerve.
Comments:
Reference: HP:0001093
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 arteriovenous malformation (HP:0031256) help
..expandOptic nerve compression (HP:0007807) help
..expandOptic nerve misrouting (HP:0025551) help
..expandOptic neuritis (HP:0100653) help
..expandOptic neuropathy (HP:0001138) help


Genes (7) :B4GAT1 BRAF CPAMD8 KIDINS220 PAX2 PEX2 PEX5

Diseases (7) :OMIM:615287 OMIM:115150 OMIM:617319 OMIM:617296 ORPHA:1475 OMIM:614866 OMIM:214110
 

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