Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bell's palsy |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Familial facial nerve palsy |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Supranuclear facial nerve paralysis |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Congenital facial nerve palsy |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Peripheral facial palsy |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Normal function of the facial nerve. |
Is a |
False |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Mild dysfunction of the facial nerve evidenced by slight facial weakness, possible mild synkinesis, normal symmetry and tone at rest, moderate to good forehead movement, complete eye closure and slight asymmetry of the mouth. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Moderate dysfunction of the facial nerve evidenced by asymmetry of the face without disfigurement, moderate synkinesis, contracture, or hemifacial spasm, normal symmetry and tone at rest, slight to moderate movement of forehead, complete eye closure with effort and slight weakness of the mouth which persists even with maximum effort. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Moderately severe dysfunction of the facial nerve evidenced by weakness and/or asymmetry of the face causing disfigurement, normal symmetry and tone at rest, absence of forehead movement, incomplete eye closure and asymmetry of the mouth even with maximum effort. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Severe dysfunction of the facial nerve evidenced by barely perceptible movement, facial asymmetry at rest, absence of forehead movement, incomplete eye closure, and only slight movement of the mouth. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Total paralysis of the facial nerve. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Deafness-ear malformation-facial palsy syndrome is characterized by profound conductive deafness due to stapedial abnormalities associated with variable malformations of the external ears and facial paralysis. It has been described in three siblings and their mother. Inheritance is autosomal dominant. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Congenital hereditary facial paralysis-variable hearing loss syndrome is an extremely rare autosomal recessive disorder characterized by bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears), and strabismus. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
History of facial palsy (situation) |
Associated finding |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
1 |
Acute mastoiditis with facial paralysis |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
A rare, localized variant of Guillain-Barré syndrome characterized by rapidly progressive bilateral facial nerve palsy, distal paresthesias, and minimal or no motor weakness. Deep tendon reflexes are usually diminished or absent but can be present or even exaggerated in rare cases. CSF analysis may reveal albuminocytologic dissociation. Nerve conduction velocity studies often show demyelinating type of neuropathy, although axonal polyneuropathy has been also described. |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|
Facial palsy as birth trauma |
Is a |
True |
Facial palsy (disorder) |
Inferred relationship |
Some |
|