Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the first metatarsal bone (HP:0010054)help
Grandparent Node:
expandDuplication of metatarsal bones (HP:0001449)help
Parent Node:
expandDuplication of the 1st metatarsal (HP:0010075)help
..Starting node
..expandComplete duplication of the 1st metatarsal (HP:0010098)help
Term ID: 10098
Name: Complete duplication of the 1st metatarsal
Synonym: Complete duplication of the 1st long bone of foot
Definition: A developmental defect consisting in the complete duplication of the first metatarsal bone.
Comments:
Reference: HP:0010098
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPartial duplication of the 1st metatarsal (HP:0010099) 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:0010098HP:0010098Complete duplication of the 1st metatarsal0 CL E G H


Genes (0) :

Diseases (0) :
 

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