Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the seventh cranial nerve (HP:0010827)help
Grandparent Node:
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Cranial nerve paralysis (HP:0006824)help
Grandparent Node:
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Muscle weakness (HP:0001324)help
Grandparent Node:
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Weakness of facial musculature (HP:0030319)help
Parent Node:
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Facial palsy (HP:0010628)help
..Starting node
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Unilateral facial palsy (HP:0012799)help
Term ID: 12799
Name: Unilateral facial palsy
Synonym: Facial droop; Paralysis of one side of the face; Unilateral facial muscle paralysis; Unilateral facial muscle weakness; Unilateral facial paralysis; Unilateral facial weakness; Weakness of one side of the face
Definition: One-sided weakness of the muscles of facial expression and eye closure.
Comments:
Reference: HP:0012799
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral facial palsy (HP:0430025) help
..expandFacial diplegia (HP:0001349) help
..expandFrontalis muscle weakness (HP:0004661) 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:0012799HP:0012799Unilateral facial palsy0HK1 CL E G H30984922OMIM:618547NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES; NEDVIBA11
HP:0012799HP:0012799Unilateral facial palsy0SUPT16H CL E G H1119811465OMIM:619480NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND THIN CORPUS CALLOSUM; NEDDFAC
HP:0012799HP:0012799Unilateral facial palsy0XRCC2 CL E G H751612829OMIM:617247FANCONI ANEMIA, COMPLEMENTATION GROUP U125


Genes (3) :HK1 SUPT16H XRCC2

Diseases (3) :OMIM:618547 OMIM:619480 OMIM:617247
 

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