Human Phenotype Ontology 
Grandparent Node:
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Syndactyly (HP:0001159)help
Parent Node:
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Finger syndactyly (HP:0006101)help
..Starting node
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2-4 finger syndactyly (HP:0010709)help
Term ID: 10709
Name: 2-4 finger syndactyly
Synonym: Syndactyly of second to fourth fingers; Webbed index through ring fingers
Definition: Syndactyly with fusion of the fingers two to four.
Comments:
Reference: HP:0010709
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 finger syndactyly (HP:0010704) help
..expand1-3 finger syndactyly (HP:0010706) help
..expand1-4 finger syndactyly (HP:0010707) help
..expand1-5 finger syndactyly (HP:0010708) help
..expand2-3 finger syndactyly (HP:0001233) help
..expand2-5 finger syndactyly (HP:0010692) help
..expand3-4 finger syndactyly (HP:0006097) help
..expand3-5 finger syndactyly (HP:0010710) help
..expand4-5 finger syndactyly (HP:0010705) help
..expandCutaneous finger syndactyly (HP:0010554) help
..expandOsseous finger syndactyly (HP:0010492) 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:0010709HP:00107092-4 finger syndactyly0CDC45 CL E G H83181739OMIM:617063Meier-Gorlin syndrome 79
HP:0010709HP:00107092-4 finger syndactyly0CDH3 CL E G H10011762OMIM:225280Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome87
HP:0010709HP:00107092-4 finger syndactyly0NECTIN4 CL E G H8160719688OMIM:613573Ectodermal dysplasia-syndactyly syndrome 17
HP:0010709HP:00107092-4 finger syndactyly0SALL1 CL E G H629910524OMIM:107480Townes-Brocks syndrome 1.124


Genes (4) :CDC45 CDH3 NECTIN4 SALL1

Diseases (4) :OMIM:617063 OMIM:225280 OMIM:613573 OMIM:107480
 

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