Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of toe (HP:0001780)help
Grandparent Node:
expandSyndactyly (HP:0001159)help
Parent Node:
expandToe syndactyly (HP:0001770)help
..Starting node
..expand1-3 toe syndactyly (HP:0001459)help
Term ID: 1459
Name: 1-3 toe syndactyly
Synonym: Webbed 1st-3rd toes
Definition: Syndactyly with fusion of toes one to three.
Comments:
Reference: HP:0001459
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 toe syndactyly (HP:0010711) help
..expand1-4 toe syndactyly (HP:0010712) help
..expand1-5 toe syndactyly (HP:0010713) help
..expand2-3 toe syndactyly (HP:0004691) help
..expand2-4 toe syndactyly (HP:0010714) help
..expand2-5 toe syndactyly (HP:0010715) help
..expand3-4 toe syndactyly (HP:0009779) help
..expand3-5 toe syndactyly (HP:0010716) help
..expand4-5 toe syndactyly (HP:0004692) help
..expandCutaneous syndactyly of toes (HP:0010621) help
..expandOsseous syndactyly of toes (HP:0010717) 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:0001459HP:00014591-3 toe syndactyly0GLI3 CL E G H27374319OMIM:175700Greig cephalopolysyndactyly syndrome270


Genes (1) :GLI3

Diseases (1) :OMIM:175700
 

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