Human Phenotype Ontology 
Grandparent Node:
expandAbnormal forearm bone morphology (HP:0040072)help
Parent Node:
expandExostoses of the forearm bones (HP:0003960)help
Parent Node:
expandobsolete Abnormality of the ulna (HP:0002997)help
..Starting node
..expandExostoses of the ulna (HP:0003985)help
Term ID: 3985
Name: Exostoses of the ulna
Synonym:
Definition:
Comments:
Reference: HP:0003985
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of ulna (HP:0040071) help
..expandAbnormal olecranon morphology (HP:0004032) help
..expandAbnormal ulnar epiphysis morphology (HP:0004037) help
..expandAbnormal ulnar metaphysis morphology (HP:0004039) help
..expandAplasia/Hypoplasia of the ulna (HP:0006495) help
..expandDorsal subluxation of ulna (HP:0006459) help
..expandFractured ulna (HP:0003987) help
..expandLong ulna (HP:0003988) help
..expandNotched ulna (HP:0003989) help
..expandOsteosclerosis of the ulna (HP:0003991) help
..expandPointed ulna (HP:0003990) help
..expandPosteriorly dislocated ulna (HP:0003984) help
..expandRadioulnar synostosis (HP:0002974) help
..expandSlender ulna (HP:0003992) help
..expandUlnar bowing (HP:0003031) 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:0003985HP:0003985Exostoses of the ulna0 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.