Facial palsy
Symptom Information:
Symptom ID: | HPO:0010628 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||||||||||||||||||||||||||
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 facial musculature(HPO:0000301) Facial palsy(HPO:0010628) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) 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) |
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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) |