Human Phenotype Ontology 
Grandparent Node:
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Abnormal scapula morphology (HP:0000782)help
Grandparent Node:
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Abnormal shoulder morphology (HP:0003043)help
Parent Node:
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Abnormality of the glenoid fossa (HP:0011912)help
..Starting node
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Flat glenoid fossa (HP:0000911)help
Term ID: 911
Name: Flat glenoid fossa
Synonym:
Definition: Abnormally flat configuration of the glenoid fossa, also known as the glenoid cavity, which is the articular surface of the scapula that articulates with the head of the humerus.
Comments:
Reference: HP:0000911
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent glenoid fossa (HP:0006591) help
..expandGlenoid fossa hypoplasia (HP:0006633) 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:0000911HP:0000911Flat glenoid fossa0DYM CL E G H5480821317OMIM:223800Dyggve-Melchior-Clausen disease.65
HP:0000911HP:0000911Flat glenoid fossa0ORC1 CL E G H49988487OMIM:224690Meier-Gorlin syndrome 1.53


Genes (2) :DYM ORC1

Diseases (2) :OMIM:223800 OMIM:224690
 

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