Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the calf (HP:0002981)help
Grandparent Node:
expandobsolete Abnormal morphology of bones of the lower limbs (HP:0040066)help
Parent Node:
expandAbnormality of fibula morphology (HP:0002991)help
Parent Node:
expandAbnormality of tibia morphology (HP:0002992)help
..Starting node
..expandTibiofibular diastasis (HP:0100535)help
Term ID: 100535
Name: Tibiofibular diastasis
Synonym:
Definition:
Comments:
Reference: HP:0100535
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal tibial metaphysis morphology (HP:0006491) help
..expandAbnormality of the tibial plateaux (HP:0003832) help
..expandAbnormality of tibial epiphyses (HP:0006508) help
..expandAplasia/Hypoplasia of the tibia (HP:0005772) help
..expandIncreased length of the tibia (HP:0010504) help
..expandMorbus Osgood-Schlatter (HP:0010890) help
..expandSynostosis involving the tibia (HP:0005929) help
..expandTibial bowing (HP:0002982) help
..expandTibial pseudarthrosis (HP:0009736) help
..expandTibial spur (HP:0031173) help
..expandTibial torsion (HP:0100694) help
..expandTriangular tibia (HP:0031260) 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:0100535HP:0100535Tibiofibular diastasis0 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.