Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the mouth (HP:0000153)help
Parent Node:
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Abnormal mandible morphology (HP:0000277)help
Parent Node:
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Abnormal oral morphology (HP:0031816)help
..Starting node
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Abnormal mandible coronoid process morphology (HP:3000078)help
Term ID: 3000078
Name: Abnormal mandible coronoid process morphology
Synonym: Abnormality of mandible coronoid process
Definition: An abnormality of a mandible coronoid process.
Comments:
Reference: HP:3000078
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal inferior alveolar artery morphology (HP:3000054) help
..expandAbnormal mandible condylar process morphology (HP:3000077) help
..expandAbnormal oral cavity morphology (HP:0000163) help
..expandOral cleft (HP:0000202) help
..expandPierre-Robin sequence (HP:0000201) 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:3000078HP:3000078Abnormal mandible coronoid process morphology0 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.