Human Phenotype Ontology 
Grandparent Node:
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Abnormality of toe (HP:0001780)help
Grandparent Node:
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Syndactyly (HP:0001159)help
Parent Node:
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Toe syndactyly (HP:0001770)help
..Starting node
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2-4 toe syndactyly (HP:0010714)help
Term ID: 10714
Name: 2-4 toe syndactyly
Synonym: Syndactyly of toes 2, 3 and 4; Syndactyly toes 2-4; Webbed 2nd-4th toes
Definition: Syndactyly with fusion of toes two to four.
Comments:
Reference: HP:0010714
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
..expand2-5 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:0010714HP:00107142-4 toe syndactyly0CKAP2L CL E G H15046826877OMIM:272440Filippi syndrome.7
HP:0010714HP:00107142-4 toe syndactyly0PIK3CA CL E G H52908975ORPHA:276280Hemihyperplasia-multiple lipomatosis syndromeHP:0040283 - Occasional162


Genes (2) :CKAP2L PIK3CA

Diseases (2) :OMIM:272440 ORPHA:276280
 

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