Human Phenotype Ontology 
Grandparent Node:
expand
Syndactyly (HP:0001159)help
Parent Node:
expand
Finger syndactyly (HP:0006101)help
..Starting node
..expand
2-5 finger syndactyly (HP:0010692)help
Term ID: 10692
Name: 2-5 finger syndactyly
Synonym: Webbed 2nd-5th fingers; Webbed index, middle and little finger; Webbed index, middle and pinkie finger; Webbed index, middle and pinky finger
Definition: Syndactyly with fusion of fingers two to five.
Comments:
Reference: HP:0010692
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
..expand2-4 finger syndactyly (HP:0010709) 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:0010692HP:00106922-5 finger syndactyly0NSDHL CL E G H5081413398OMIM:308050Congenital hemidysplasia with ichthyosiform erythroderma and limb defects34
HP:0010692HP:00106922-5 finger syndactyly0RTTN CL E G H2591418654ORPHA:468631Microcephalic cortical malformations-short stature due to RTTN deficiencyHP:0040283 - Occasional113


Genes (2) :NSDHL RTTN

Diseases (2) :OMIM:308050 ORPHA:468631
 

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