Human Phenotype Ontology 
Grandparent Node:
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Abnormal thorax morphology (HP:0000765)help
Parent Node:
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Abnormal rib cage morphology (HP:0001547)help
..Starting node
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Abnormal facility in opposing the shoulders (HP:0005259)help
Term ID: 5259
Name: Abnormal facility in opposing the shoulders
Synonym:
Definition: Increased range of shoulder movement related to aplasia or hypoplasia of the clavicles that results in the ability to approximate the shoulders in front of the chest.
Comments:
Reference: HP:0005259
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal rib morphology (HP:0000772) help
..expandAsymmetry of the thorax (HP:0001555) help
..expandBell-shaped thorax (HP:0001591) help
..expandDeformed rib cage (HP:0000886) help
..expandEnlarged thorax (HP:0100625) help
..expandRestricted chest movement (HP:0006596) help
..expandThoracic dysplasia (HP:0006644) 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:0005259HP:0005259Abnormal facility in opposing the shoulders0RUNX2 CL E G H86010472OMIM:119600Cleidocranial dysplasia.90


Genes (1) :RUNX2

Diseases (1) :OMIM:119600
 

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