Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Ophthalmoparesis (HP:0000597)help
..Starting node
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Static ophthalmoparesis (HP:0008507)help
Term ID: 8507
Name: Static ophthalmoparesis
Synonym:
Definition:
Comments:
Reference: HP:0008507
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandOculomotor nerve palsy (HP:0012246) help
..expandOphthalmoplegia (HP:0000602) help
..expandSetting-sun eye phenomenon (HP:0012470) help
..expandWeak extraocular muscles (HP:0007715) 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:0008507HP:0008507Static ophthalmoparesis0 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.