Facial palsy

Symptom Information:

Symptom ID: HPO:0010628
Synonyms:
Bell's palsy [HPO:0010628]
Cranial nerve VII palsy [HPO:0010628]
Facial muscle weakness [HPO:0010628]
Facial muscle weakness of muscles innervated by CN VII [HPO:0010628]
Facial nerve palsy [HPO:0010628]
Facial nerve paralysis [HPO:0010628]
Facial palsy, unilateral or bilateral [HPO:0010628]
Facial weakness [HPO:0010628]
Seventh cranial nerve palsy [HPO:0010628]
VII th cranial nerve palsy [HPO:0010628]
Facial nerve palsy [Orphanet:3280]
Cranial nerve palsy [Orphanet:43020]
Facial palsy (disorder) [Orphanet:3280]
Facial paralysis [Orphanet:3280]
Cranial nerve palsies [Orphanet:43020]
Cranial nerve VII palsy [OMIM:Cranial nerve VII palsy]
Facial muscle weakness [OMIM:Facial muscle weakness]
Facial muscle weakness of muscles innervated by CN VII [OMIM:Facial muscle weakness of muscles innervated by CN VII]
Facial palsy [OMIM:Facial palsy]
Facial palsy, unilateral or bilateral [OMIM:Facial palsy, unilateral or bilateral]
Facial weakness [OMIM:Facial weakness]
Facial palsy [Orphanet:3280]
Cranial nerves palsy [Orphanet:43020]
Paralysis facial [Orphanet:3280]
Cranial nerve paralysis [Orphanet:43020]
VIIth nerve paralysis [MedDRA:10050040]
Bell's palsy [MedDRA:10050040]
Facial droop [MedDRA:10050040]
Facial palsy [MedDRA:10050040]
Facial paralysis [MedDRA:10050040]
LMNL of VIIth nerve [MedDRA:10050040]
Palsy Bells [MedDRA:10050040]
Paralysis facial [MedDRA:10050040]
UMNL of VIIth nerve [MedDRA:10050040]
Facial palsy aggravated [MedDRA:10050040]
VIIth nerve palsy [MedDRA:10050040]
Cranial nerve paralysis [MedDRA:10061908]
Paralysis of cranial nerve NOS [MedDRA:10061908]
Facial nerve palsy [OMIM:Facial nerve palsy]
Facial nerve palsy (cranial nerve VII) [OMIM:Facial nerve palsy (cranial nerve VII)]
Facial nerve paralysis (10% of patients) [OMIM:Facial nerve paralysis (10% of patients)]
Facial weakness (in some) [OMIM:Facial weakness (in some)]
Facial weakness (less common) [OMIM:Facial weakness (less common)]
Quality:
Cross references:
HPO:0006824 "Cranial nerve paralysis" [Orphanet:43020]
Orphanet:3280 "Facial palsy" [Orphanet:3280]
Orphanet:43020 "Cranial nerves palsy" [Orphanet:43020]
OMIM: "Cranial nerve VII palsy" [OMIM:Cranial nerve VII palsy]
OMIM: "Facial muscle weakness" [OMIM:Facial muscle weakness]
OMIM: "Facial muscle weakness of muscles innervated by CN VII" [OMIM:Facial muscle weakness of muscles innervated by CN VII]
OMIM: "Facial palsy" [OMIM:Facial palsy]
OMIM: "Facial palsy, unilateral or bilateral" [OMIM:Facial palsy, unilateral or bilateral]
OMIM: "Facial weakness" [OMIM:Facial weakness]
OMIM: "Facial nerve palsy" [OMIM:Facial nerve palsy]
OMIM: "Facial nerve palsy (cranial nerve VII)" [OMIM:Facial nerve palsy (cranial nerve VII)]
OMIM: "Facial nerve paralysis (10% of patients)" [OMIM:Facial nerve paralysis (10% of patients)]
OMIM: "Facial weakness (in some)" [OMIM:Facial weakness (in some)]
OMIM: "Facial weakness (less common)" [OMIM:Facial weakness (less common)]
UMLS:C0015469 "Facial paralysis" [Orphanet:3280]
UMLS:C0151311 "Cranial nerve palsies" [Orphanet:43020]
Is a (Direct Parents):
HPO         Muscle weakness
Orphanet Abnormal facial shape
Orphanet Functional anomalies of the nervous system
MedDRA Facial cranial nerve disorders
HPO         Bilateral facial palsy
HPO         Abnormality of facial musculature
HPO         Cranial nerve paralysis
HPO         Abnormality of the seventh cranial nerve
HPO         Unilateral facial palsy
MedDRA Cranial nerve disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormality of the cranial nerves(HPO:0001291)
                   Cranial nerve paralysis(HPO:0006824)
                      Facial palsy(HPO:0010628)
                   Abnormality of the seventh cranial nerve(HPO:0010827)
                      Facial palsy(HPO:0010628)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Facial palsy(HPO:0010628)
          Abnormality of facial musculature(HPO:0000301)
             Facial palsy(HPO:0010628)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of facial soft tissue(HPO:0011799)
                   Abnormality of facial musculature(HPO:0000301)
                      Facial palsy(HPO:0010628)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Cranial nerve disorders (excl neoplasms)(MedDRA:10011305)
       Cranial nerve disorders NEC(MedDRA:10011306)
          Facial palsy(HPO:0010628)
       Facial cranial nerve disorders(MedDRA:10016054)
          Facial palsy(HPO:0010628)
Database Frequency: 146 / 7739
Resource:

All diseases associated with this symptom:

2p15p16.1 microdeletion syndrome (Orphanet:261349)
AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA (OMIM:107550)
Acro-renal-ocular syndrome (Orphanet:959)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alexander disease (Orphanet:58)
Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant centronuclear myopathy (Orphanet:169189)
Autosomal dominant osteosclerosis, Worth type (Orphanet:2790)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency (Orphanet:363543)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Autosomal recessive limb-girdle muscular dystrophy type 2L (Orphanet:206549)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
BOR syndrome (Orphanet:107)
BRANCHIOOTORENAL SYNDROME 1 (OMIM:113650)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Blau syndrome (Orphanet:90340)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Branchio-otic syndrome (Orphanet:52429)
CADASIL (Orphanet:136)
CHARGE syndrome (Orphanet:138)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24 (OMIM:616239)
CRANIAL NERVES, CONGENITAL PARESIS OF (OMIM:218100)
CRANIAL NERVES, RECURRENT PARESIS OF (OMIM:218200)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:123000)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Camurati-Engelmann disease (Orphanet:1328)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Catel-Manzke syndrome (Orphanet:1388)
Charcot-Marie-Tooth disease type 4B1 (Orphanet:99955)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)
Circumscribed cutaneous aplasia of the vertex (Orphanet:1114)
Classic multiminicore myopathy (Orphanet:324604)
Cold-induced sweating syndrome (Orphanet:157820)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
Congenital hereditary facial paralysis with variable hearing loss (Orphanet:306530)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect (Orphanet:280671)
Congenital muscular dystrophy type 1B (Orphanet:98893)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
Craniometaphyseal dysplasia (Orphanet:1522)
Cystinosis (Orphanet:213)
Deafness - ear malformation - facial palsy (Orphanet:3232)
Desmin-related myopathy with Mallory body-like inclusions (Orphanet:84132)
Desminopathy (Orphanet:98909)
Early-onset myopathy with fatal cardiomyopathy (Orphanet:289377)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
FACIAL PARESIS, HEREDITARY CONGENITAL, 2 (OMIM:604185)
FACIAL PARESIS, HEREDITARY CONGENITAL, 3 (OMIM:614744)
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2 (OMIM:158901)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
Facial asymmetry - temporal seizures (Orphanet:1167)
Facioscapulohumeral dystrophy (Orphanet:269)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial recurrent peripheral facial palsy (Orphanet:2809)
Gaucher disease (Orphanet:355)
Giant axonal neuropathy (Orphanet:643)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
HYPEROSTOSIS CRANIALIS INTERNA (OMIM:144755)
Hereditary myoclonus - progressive distal muscular atrophy (Orphanet:2590)
Hyperostosis corticalis generalisata (Orphanet:3416)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 (OMIM:167320)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
Infantile Refsum disease (Orphanet:772)
Infantile axonal neuropathy (Orphanet:2679)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated hereditary congenital facial paralysis (Orphanet:306527)
Laing distal myopathy (Orphanet:59135)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE (OMIM:609456)
MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEMATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS (OMIM:601170)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYASTHENIA GRAVIS (OMIM:254200)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 12 (OMIM:610542)
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL (OMIM:608930)
MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL (OMIM:616313)
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL (OMIM:616322)
MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616323)
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL (OMIM:616324)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
MYASTHENIC SYNDROME, CONGENITAL, 8 (OMIM:615120)
MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616325)
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET (OMIM:614399)
MYOPATHY, CENTRONUCLEAR, 1 (OMIM:160150)
MYOPATHY, CENTRONUCLEAR, 5 (OMIM:615959)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED (OMIM:300580)
MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT (OMIM:616209)
Melkersson-Rosenthal syndrome (Orphanet:2483)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (Orphanet:254864)
Moebius syndrome (Orphanet:570)
Muscular dystrophy - white matter spongiosis (Orphanet:1877)
Muscular dystrophy, Selcen type (Orphanet:199340)
Myopathy and diabetes mellitus (Orphanet:2596)
Myosclerosis (Orphanet:289380)
NEMALINE MYOPATHY 10 (OMIM:616165)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 8 (OMIM:615348)
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB (OMIM:607641)
Nemaline myopathy (Orphanet:607)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neurofibromatosis type 2 (Orphanet:637)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4 (OMIM:611490)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8 (OMIM:615085)
Oculopharyngeal muscular dystrophy (Orphanet:270)
Oculopharyngodistal myopathy (Orphanet:98897)
Okihiro syndrome (Orphanet:93293)
Ophthalmoplegia - intellectual deficit - lingua scrotalis (Orphanet:2743)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Osteosclerosis - developmental delay - craniosynostosis (Orphanet:178377)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 2 (OMIM:609283)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Pelizaeus-Merzbacher-like due to GJC2 mutation (Orphanet:280282)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pontine tegmental cap dysplasia (Orphanet:269229)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Riboflavin transporter deficiency (Orphanet:97229)
Rigid spine syndrome (Orphanet:97244)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SCLEROSTEOSIS 2 (OMIM:614305)
Sclerosteosis (Orphanet:3152)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Sneddon syndrome (Orphanet:820)
Steinert myotonic dystrophy (Orphanet:273)
Syngnathia multiple anomalies (Orphanet:3262)
Wildervanck syndrome (Orphanet:3456)
X-linked centronuclear myopathy (Orphanet:596)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)