Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal conjugate eye movement (HP:0000549)help
Parent Node:
expand
Strabismus (HP:0000486)help
..Starting node
..expand
obsolete Congenital strabismus (HP:0000487)help
Term ID: 487
Name: obsolete Congenital strabismus
Synonym:
Definition:
Comments:
Reference: HP:0000487
Genes and Diseases:
 
       Child Nodes:
........expandCongenital exotropia (HP:0008033) help

 Sister Nodes: 
..expandConcomitant strabismus (HP:0025069) help
..expandCyclodeviation (HP:0025589) help
..expandEsodeviation (HP:0020045) help
..expandExodeviation (HP:0020049) help
..expandHyperdeviation (HP:0025587) help
..expandHypodeviation (HP:0025588) help
..expandIncomitant strabismus (HP:0025068) help
..expandMicrotropia (HP:0031724) help
..expandMonocular strabismus (HP:0010877) help
..expandNeurogenic strabismus (HP:0031775) 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:0000487HP:0000487obsolete Congenital strabismus0 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.