Human Phenotype Ontology 
Grandparent Node:
expandEsotropia (HP:0000565)help
Parent Node:
expandNon-accomodative esotropia (HP:0031760)help
..Starting node
..expandInfantile constant esotropia (HP:0031761)help
Term ID: 31761
Name: Infantile constant esotropia
Synonym: Infantile (constant) esotropia
Definition: Constant esotropia occurring before 6 months of age. It is typically associated with a large angle of deviation, alternating fixation (therefore low risk of amblyopia) and poor potential for binocular single vision. Other features that might be present in individuals with infantile (constant) esotropia include latent nystagmus or manifest latent nystagmus, dissociated vertical divergence, cyclotropia, abnormal head posture, limited abduction.
Comments:
Reference: HP:0031761
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBasic constant esotropia (HP:0031759) help
..expandCyclic esotropia (HP:0031763) help
..expandDistance esotropia (HP:0031762) help
..expandNear esotropia (HP:0031722) 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:0031761HP:0031761Infantile constant esotropia0 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.