Human Phenotype Ontology 
Grandparent Node:
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Strabismus (HP:0000486)help
Parent Node:
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Hyperdeviation (HP:0025587)help
..Starting node
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Hypertropia (HP:0025586)help
Term ID: 25586
Name: Hypertropia
Synonym:
Definition: A type of strabismus characterized by permanent upward deviation of the visual axis of one eye.
Comments:
Reference: HP:0025586
Genes and Diseases:
 
       Child Nodes:
........expandAlternating hypetropia (HP:0500076) help

 Sister Nodes: 
..expandHyperphoria (HP:0025585) 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:0025586HP:0025586Hypertropia0FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361
HP:0025586HP:0025586Hypertropia0PHOX2A CL E G H401691OMIM:602078Fibrosis of extraocular muscles, congenital, 2.6
HP:0025586HP:0025586Hypertropia0SALL2 CL E G H629710526OMIM:216820COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE1
HP:0025586HP:0500076Alternating hypertropia1 CL E G H


Genes (3) :FBN1 PHOX2A SALL2

Diseases (3) :OMIM:154700 OMIM:602078 OMIM:216820
 

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