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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Abnormality of frontalis muscle belly (HP:3000004)help
Parent Node:
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Facial palsy (HP:0010628)help
..Starting node
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Frontalis muscle weakness (HP:0004661)help
Term ID: 4661
Name: Frontalis muscle weakness
Synonym: Weak frontalis muscle; Weakness of forehead muscle
Definition: Reduced strength of the frontalis muscle (which is located on the forehead).
Comments:
Reference: HP:0004661
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilateral facial palsy (HP:0430025) help
..expandFacial diplegia (HP:0001349) help
..expandUnilateral facial palsy (HP:0012799) 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:0004661HP:0004661Frontalis muscle weakness0AGRN CL E G H375790329ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent127
HP:0004661HP:0004661Frontalis muscle weakness0CHAT CL E G H11031912ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent65
HP:0004661HP:0004661Frontalis muscle weakness0COL13A1 CL E G H13052190ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent6
HP:0004661HP:0004661Frontalis muscle weakness0MYO9A CL E G H46497608ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent
HP:0004661HP:0004661Frontalis muscle weakness0SLC18A3 CL E G H657210936ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent2
HP:0004661HP:0004661Frontalis muscle weakness0SLC25A1 CL E G H657610979ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent28
HP:0004661HP:0004661Frontalis muscle weakness0SLC5A7 CL E G H6048214025ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent9
HP:0004661HP:0004661Frontalis muscle weakness0SNAP25 CL E G H661611132ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent2
HP:0004661HP:0004661Frontalis muscle weakness0SYT2 CL E G H12783311510ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent4
HP:0004661HP:0004661Frontalis muscle weakness0VAMP1 CL E G H684312642ORPHA:98914Presynaptic congenital myasthenic syndromesHP:0040281 - Very frequent2


Genes (10) :AGRN CHAT COL13A1 MYO9A SLC18A3 SLC25A1 SLC5A7 SNAP25 SYT2 VAMP1

Diseases (1) :ORPHA:98914
 

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