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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4-5 toe syndactyly (HP:0004692)help
Term ID: 4692
Name: 4-5 toe syndactyly
Synonym: Symmetric syndactyly, toes 4 and 5; Syndactyly of toes 4 and 5; Webbed 4th-5th toes
Definition: Syndactyly with fusion of toes four and five.
Comments:
Reference: HP:0004692
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
..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:0004692HP:00046924-5 toe syndactyly0HOXD13 CL E G H3239186300Syndactyly, type V186300C1861348OMIM142715136142989
HP:0004692HP:00046924-5 toe syndactyly0HOXD13 CL E G H3239186000Synpolydactyly 1186000C2699746OMIM142715136142989
HP:0004692HP:00046924-5 toe syndactyly0RBBP8 CL E G H5932251255Microcephaly with mental retardation and digital anomalies251255C0796063OMIM161089891604124
HP:0004692HP:00046924-5 toe syndactyly0TBX15 CL E G H6913260660Cousin syndrome260660C1850040OMIM153811594604127
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004692HP:00046924-5 toe syndactyly0MYCN CL E G H4613164280Feingold syndrome 1164280C0796068OMIM0461037559164840


Genes (4) :HOXD13 MYCN RBBP8 TBX15

Diseases (5) :186300 186000 164280 251255 260660
 

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