Human Phenotype Ontology 
Grandparent Node:
expandAbnormal epiphysis morphology (HP:0005930)help
Parent Node:
expandPremature epimetaphyseal fusion (HP:0010588)help
..Starting node
..expandPremature epimetaphyseal fusion in fibula (HP:0012565)help
Term ID: 12565
Name: Premature epimetaphyseal fusion in fibula
Synonym:
Definition: Stop of growth at the epiphyseal plate the hyaline cartilage plate in the metaphysis at one or more long bones in the fibula, at an earlier than normal age, resulting in growth arrest and shortening of the involved bone.
Comments:
Reference: HP:0012565
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPremature epimetaphyseal fusion in foot (HP:0012563) help
..expandPremature epimetaphyseal fusion in hand (HP:0012562) help
..expandPremature epimetaphyseal fusion in radius (HP:0012566) help
..expandPremature epimetaphyseal fusion in tibia (HP:0012564) help
..expandPremature epimetaphyseal fusion in ulna (HP:0012567) 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:0012565HP:0012565Premature epimetaphyseal fusion in fibula0 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.