Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of toe (HP:0001780)help
Grandparent Node:
expandDuplication involving bones of the feet (HP:0009136)help
Grandparent Node:
expandPolydactyly (HP:0010442)help
Parent Node:
expandFoot polydactyly (HP:0001829)help
..Starting node
..expandEctopic accesory toe-like appendage (HP:0010440)help
Term ID: 10440
Name: Ectopic accesory toe-like appendage
Synonym:
Definition: In contrast to forms of polydactyly where the supernumerary digit (this can either be a rudimentary or a completely 'normal' digit) is either located postaxial (on the fibular side of the foot, next top the little toe), preaxial (on the tibial side of the foot, next to the big toe) or mesoaxial (somewhere central, between big and little toe), a supernumerary digit may also be placed ectopically, meaning anywhere else except post-,meso- or preaxial. In the literature this is sometimes referred to as Disorganisation-like Syndrome (OMIM223200).
Comments:
Reference: HP:0010440
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMesoaxial foot polydactyly (HP:0010112) help
..expandMirror image foot polydactyly (HP:0010691) help
..expandPostaxial foot polydactyly (HP:0001830) help
..expandPreaxial foot polydactyly (HP:0001841) 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:0010440HP:0010440Ectopic accesory toe-like appendage0 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.