Human Phenotype Ontology 
Grandparent Node:
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Ophthalmoparesis (HP:0000597)help
Parent Node:
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Ophthalmoplegia (HP:0000602)help
..Starting node
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Progressive ophthalmoplegia (HP:0007650)help
Term ID: 7650
Name: Progressive ophthalmoplegia
Synonym:
Definition:
Comments:
Reference: HP:0007650
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExternal ophthalmoplegia (HP:0000544) help
..expandInternal ophthalmoplegia (HP:0007942) help
..expandInternuclear ophthalmoplegia (HP:0030773) help
..expandSupranuclear ophthalmoplegia (HP:0000623) help
..expandTotal ophthalmoplegia (HP:0007824) 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:0007650HP:0007650Progressive ophthalmoplegia0ROBO3 CL E G H6422113433OMIM:607313Gaze palsy, familial horizontal, with progressive scoliosis, 1.90


Genes (1) :ROBO3

Diseases (1) :OMIM:607313
 

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