Human Phenotype Ontology 
Grandparent Node:
expandAbnormal upper limb bone morphology (HP:0040070)help
Grandparent Node:
expandAbnormality of the upper arm (HP:0001454)help
Parent Node:
expandAbnormality of the humerus (HP:0003063)help
..Starting node
..expandOsteoporotic humerus (HP:0003876)help
Term ID: 3876
Name: Osteoporotic humerus
Synonym:
Definition:
Comments:
Reference: HP:0003876
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal humeral metaphysis morphology (HP:0003907) help
..expandAbnormal humeral ossification (HP:0012791) help
..expandAbnormal humerus morphology (HP:0031095) help
..expandAbnormality of the humeral epiphysis (HP:0003891) help
..expandAplasia/hypoplasia of the humerus (HP:0006507) help
..expandHumeral sclerosis (HP:0003881) help
..expandHumeroradial synostosis (HP:0003041) help
..expandPeriosteal new bone of humerus (HP:0003878) help
..expandScapulohumeral synostosis (HP:0006595) help
..expandTriangular humerus (HP:0003884) 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:0003876HP:0003876Osteoporotic humerus0 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.