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
..expandOsseous syndactyly of toes (HP:0010717)help
Term ID: 10717
Name: Osseous syndactyly of toes
Synonym: Osseous syndactyly of the toes
Definition: Webbing or fusion of the toes, involving soft parts and including fusion of individual bones of the toes. Bony fusions are referred to as "bony" Syndactyly if the fusion occurs in a tibial-fibular axis. Fusions of bones of the toes in a proximo-distal axis are referred to as "Symphalangism".
Comments:
Reference: HP:0010717
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 toe syndactyly (HP:0010711) help
..expand1-3 toe syndactyly (HP:0001459) 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
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010717HP:0010717Osseous syndactyly of toes0 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.