Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the epiphyses of the hallux (HP:0010056)help
Parent Node:
expandAbnormality of the epiphysis of the 1st metatarsal (HP:0010125)help
..Starting node
..expandPseudoepiphysis of the 1st metatarsal (HP:0010156)help
Term ID: 10156
Name: Pseudoepiphysis of the 1st metatarsal
Synonym:
Definition:
Comments:
Reference: HP:0010156
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent epiphysis of the 1st metatarsal (HP:0010149) help
..expandBracket epiphysis of the 1st metatarsal (HP:0010150) help
..expandCone-shaped epiphysis of the 1st metatarsal (HP:0010151) help
..expandEnlarged epiphysis of the 1st metatarsal (HP:0010152) help
..expandFragmentation of the epiphysis of the 1st metatarsal (HP:0010153) help
..expandIrregular epiphysis of the 1st metatarsal (HP:0010154) help
..expandIvory epiphysis of the 1st metatarsal (HP:0010155) help
..expandSmall epiphysis of the 1st metatarsal (HP:0010157) help
..expandStippling of the epiphysis of the 1st metatarsal (HP:0010158) help
..expandTriangular epiphysis of the 1st metatarsal (HP:0010159) 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:0010156HP:0010156Pseudoepiphysis 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.