Human Phenotype Ontology 
Grandparent Node:
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Abnormal foot morphology (HP:0001760)help
Grandparent Node:
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Abnormal lower limb bone morphology (HP:0040069)help
Parent Node:
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Abnormal metatarsal morphology (HP:0001832)help
Parent Node:
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Duplication involving bones of the feet (HP:0009136)help
..Starting node
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Duplication of metatarsal bones (HP:0001449)help
Term ID: 1449
Name: Duplication of metatarsal bones
Synonym: Duplication of long bones of foot
Definition:
Comments:
Reference: HP:0001449
Genes and Diseases:
 
       Child Nodes:
........expandDuplication of the 1st metatarsal (HP:0010075) help
................... HP:0010098 Complete duplication of the 1st metatarsal
................... HP:0010099 Partial duplication of the 1st metatarsal

 Sister Nodes: 
..expandBifid distal phalanx of toe (HP:0001853) help
..expandFoot polydactyly (HP:0001829) 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:0001449HP:0001449Duplication of metatarsal bones0 CL E G H
HP:0001449HP:0010075Duplication of the 1st metatarsal1 CL E G H
HP:0001449HP:0010098Complete duplication of the 1st metatarsal2 CL E G H
HP:0001449HP:0010099Partial duplication of the 1st metatarsal2 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.