Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the upper limb (HP:0002817)help
Grandparent Node:
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obsolete Anomaly of the limb diaphyses morphology (HP:0006504)help
Parent Node:
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Abnormal humerus morphology (HP:0031095)help
Parent Node:
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Anomaly of the upper limb diaphyses (HP:0009808)help
..Starting node
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Abnormal humeral diaphysis morphology (HP:0003926)help
Term ID: 3926
Name: Abnormal humeral diaphysis morphology
Synonym: Abnormality of shaft of long bone in upper arm; Abnormality of the humeral diaphysis
Definition: An anomaly of the humeral diaphysis.
Comments:
Reference: HP:0003926
Genes and Diseases:
 
       Child Nodes:
........expandAbnormality of the deltoid tuberosities (HP:0003889) help
................... HP:0003890 Prominent deltoid tuberosities
........expandCortical irregularity of humeral diaphysis (HP:0003927) help
........expandCortical thickening of humeral diaphysis (HP:0003928) help
........expandGround glass opacity of humeral diaphysis (HP:0003929) help
........expandLytic defects of humeral diaphysis (HP:0003930) help
........expandPeriosteal new bone of humeral diaphysis (HP:0003931) help
........expandSclerotic foci of humeral diaphysis (HP:0003932) help
........expandSclerosis of humeral diaphysis (HP:0003933) help
........expandSlender humeral diaphysis (HP:0003934) help
........expandWide humeral diaphysis (HP:0003935) help

 Sister Nodes: 
..expandAbnormal hand diaphysis morphology (HP:0005925) help
..expandAbnormality of radial diaphysis (HP:0004027) help
..expandBroad diaphyses of the upper limbs (HP:0003861) help
..expandCortical diaphyseal irregularity of the upper limbs (HP:0003858) help
..expandCortical diaphyseal thickening of the upper limbs (HP:0003859) help
..expandDiaphyseal sclerosis of the upper limbs (HP:0003860) help


Genes (1) :PRKG2

Diseases (1) :OMIM:619636
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.