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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1-5 toe syndactyly (HP:0010713)help
Term ID: 10713
Name: 1-5 toe syndactyly
Synonym: Syndactyly of all toes; Webbed 1st-5th toes
Definition: Syndactyly with fusion of toes one to five (complete syndactyly of all toes of the foot).
Comments:
Reference: HP:0010713
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
..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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0010713HP:00107131-5 toe syndactyly0GLI3 CL E G H2737174700Preaxial polydactyly 4174700C1868111OMIM12445374319165240
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :GLI3

Diseases (1) :174700
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.