Human Phenotype Ontology 
Grandparent Node:
expandStrabismus (HP:0000486)help
Parent Node:
expandIncomitant strabismus (HP:0025068)help
..Starting node
..expandBrown anomaly (HP:0031622)help
Term ID: 31622
Name: Brown anomaly
Synonym: Brown syndrome
Definition: An ocular motility defect where the affected eye(s) does not elevate in adduction but has full depression in adduction. It can be congenital or acquired from injury to or defect of the superior oblique tendon or trochlea and has a positive forced duction test result.
Comments:
Reference: HP:0031622
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDouble depressor palsy (HP:0020042) help
..expandDouble elevator palsy (HP:0020041) help
..expandDuane anomaly (HP:0009921) help
..expandHorizontal incomitant strabismus (HP:0020044) help
..expandVertical incomitant strabismus (HP:0020043) 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:0031622HP:0031622Brown anomaly0 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.