Human Phenotype Ontology 
Grandparent Node:
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Neoplasm of the skeletal system (HP:0010622)help
Parent Node:
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Abnormal scapula morphology (HP:0000782)help
Parent Node:
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Exostoses (HP:0100777)help
..Starting node
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Scapular exostoses (HP:0000918)help
Term ID: 918
Name: Scapular exostoses
Synonym: Scapulae exostoses; Shoulder bone exostoes
Definition: The presence of multiple exostoses on the scapula. An exostosis is a benign growth the projects outward from the bone surface. It is capped by cartilage.
Comments:
Reference: HP:0000918
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExostoses of hand bones (HP:0004276) help
..expandExostoses of the forearm bones (HP:0003960) help
..expandExostosis of the external auditory canal (HP:0004459) help
..expandMultiple exostoses (HP:0002762) help
..expandPelvic bone exostoses (HP:0003276) help
..expandRib exostoses (HP:0000896) 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:0000918HP:0000918Scapular exostoses0EXT1 CL E G H21313512OMIM:133700Exostoses, multiple, type I.96
HP:0000918HP:0000918Scapular exostoses0EXT1 CL E G H21313512ORPHA:321Multiple osteochondromasHP:0040284 - Very rare96
HP:0000918HP:0000918Scapular exostoses0EXT2 CL E G H21323513OMIM:133701Exostoses, multiple, type II.102
HP:0000918HP:0000918Scapular exostoses0EXT2 CL E G H21323513ORPHA:321Multiple osteochondromasHP:0040284 - Very rare102


Genes (2) :EXT1 EXT2

Diseases (3) :OMIM:133700 ORPHA:321 OMIM:133701
 

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