Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the elbow (HP:0009811)help
Grandparent Node:
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Synostosis involving bones of the upper limbs (HP:0100238)help
Parent Node:
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Abnormality of the humeroulnar joint (HP:0100745)help
Parent Node:
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Synostosis involving the elbow (HP:0003938)help
..Starting node
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Humeroulnar synostosis (HP:0003939)help
Term ID: 3939
Name: Humeroulnar synostosis
Synonym: Humeral ulnar synostosis
Definition: An abnormal osseous union (fusion) between the ulna and the humerus.
Comments:
Reference: HP:0003939
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHumeroradial synostosis (HP:0003041) 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:0003939HP:0003939Humeroulnar synostosis0 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.