Human Phenotype Ontology 
Grandparent Node:
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Cutaneous syndactyly (HP:0012725)help
Grandparent Node:
expand
Toe syndactyly (HP:0001770)help
Parent Node:
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Cutaneous syndactyly of toes (HP:0010621)help
..Starting node
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1-2 toe complete cutaneous syndactyly (HP:0005767)help
Term ID: 5767
Name: 1-2 toe complete cutaneous syndactyly
Synonym:
Definition:
Comments:
Reference: HP:0005767
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand2-3 toe cutaneous syndactyly (HP:0005709) help
..expand2-4 toe cutaneous syndactyly (HP:0005768) 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:0005767HP:00057671-2 toe complete cutaneous syndactyly0MAP3K20 CL E G H5177617797ORPHA:488232Split-foot malformation-mesoaxial polydactyly syndrome2


Genes (1) :MAP3K20

Diseases (1) :ORPHA:488232
 

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