Human Phenotype Ontology 
Grandparent Node:
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Abnormal metatarsal morphology (HP:0001832)help
Parent Node:
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Abnormality of metatarsal epiphysis (HP:0010630)help
Parent Node:
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Abnormality of the epiphysis of the 1st metatarsal (HP:0010125)help
Parent Node:
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Abnormality of the first metatarsal bone (HP:0010054)help
..Starting node
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Cone-shaped epiphysis of the 1st metatarsal (HP:0010151)help
Term ID: 10151
Name: Cone-shaped epiphysis of the 1st metatarsal
Synonym: Cone-shaped end part of the 1st long bone of foot
Definition: A conical (cone-shaped) appearance of the epiphysis of the first metatarsal of the foot.
Comments:
Reference: HP:0010151
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia/hypoplasia of the 1st metatarsal (HP:0010067) help
..expandBroad first metatarsal (HP:0010068) help
..expandBullet-shaped 1st metatarsal (HP:0010069) help
..expandCurved 1st metatarsal (HP:0010070) help
..expandDuplication of the 1st metatarsal (HP:0010075) help
..expandOsteolytic defects of the 1st metatarsal (HP:0010071) help
..expandPatchy sclerosis of the 1st metatarsal (HP:0010072) help
..expandShort first metatarsal (HP:0010105) help
..expandSynostosis involving the 1st metatarsal (HP:0010073) help
..expandTriangular shaped 1st metatarsal (HP:0010074) 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:0010151HP:0010151Cone-shaped epiphysis 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.