Human Phenotype Ontology 
Grandparent Node:
expandCraniofacial hyperostosis (HP:0004493)help
Parent Node:
expandFacial hyperostosis (HP:0005465)help
..Starting node
..expandFacial palsy secondary to cranial hyperostosis (HP:0007285)help
Term ID: 7285
Name: Facial palsy secondary to cranial hyperostosis
Synonym: Facial palsy caused by enlargement of cranial bones; Facial palsy caused by excessive growth of facial bones; Facial palsy caused by overgrowth of cranial bones; Facial palsy secondary to hypertrophy of cranial bones
Definition: Paralysis of the facial nerves on the basis of overgrowth of the cranial bones causing impingement upon the seventh cranial nerve.
Comments:
Reference: HP:0007285
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMandibular hyperostosis (HP:0004472) 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:0007285HP:0007285Facial palsy secondary to cranial hyperostosis0SOST CL E G H5096413771OMIM:269500Sclerosteosis 1.26


Genes (1) :SOST

Diseases (1) :OMIM:269500
 

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