Human Phenotype Ontology 
Grandparent Node:
expandExternal ophthalmoplegia (HP:0000544)help
Parent Node:
expandRestrictive external ophthalmoplegia (HP:0007936)help
..Starting node
..expandRestrictive partial external ophthalmoplegia (HP:0007867)help
Term ID: 7867
Name: Restrictive partial external ophthalmoplegia
Synonym:
Definition: Fibrosis of only some of the external ocular muscles such that the eyes of affected individuals are partially or completely fixed in a strabismic position.
Comments:
Reference: HP:0007867
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007867HP:0007867Restrictive partial external ophthalmoplegia0 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.