Tetanus

Tetanus is an infectious disease caused by the anaerobic bacterium <i>Clostridium tetani</i> and characterized by spasms and contractions of the skeletal muscles.



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Total: 498 (papers)

   


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
1
(65.5%)		 8723066
 Autosomal recessive disorder with muscle contractions resembling neonatal tetanus, characteristic face, camptodactyly, hyperthermia, and sudden death: a new syndrome?
Crisponi G.
Am J Med Genet. 1996;62(4):365-71.
Trismus Long philtrum Bilateral camptodactyly
rs137853143
Chromosome Aberrations Facial Muscles Fatal Outcome Females Fever Fingers Genes, Recessive Homo sapiens Infant, Newborn Male Muscle Contraction Myopathy Syndrome Tetanus Trismus
2
(45.4%)		 3156623
 Tetanus associated with dental sepsis.
Babajews A, Nicholls MW.
Br J Oral Maxillofac Surg. 1985;23(1):36-40.
Trismus Carious teeth
Bacterial Infections Deglutition Disorders Differential Diagnosis Females Homo sapiens Tetanus Tongue Trismus
3
(43.9%)		 28108438
 Cephalic tetanus as a differential diagnosis of facial nerve palsy.
Kotani Y, Kubo K, Otsu S, Tsujimoto T.
BMJ Case Rep. 2017;2017:.
Trismus Risus sardonicus
Accidental Falls Delayed Diagnosis Differential Diagnosis Encephalitis Facial Nerve Diseases Homo sapiens Laceration Male Meningitis Tetanus Trismus
3
(43.9%)		 27940761
 Tetanus and Occam's Razor: Almost Forgotten but Not Gone: A Case Report.
Skuby SO, Rhee E, Thilo EH, Simoes EA.
Pediatrics. 2016;138(5):.
Trismus Risus sardonicus
Delayed Diagnosis Fatigue Homo sapiens Infant Male Muscle Hypertonia Tetanus Trismus
3
(43.9%)		 21924448
 [Cephalic tetanus revealed by peripheral facial palsy].
Hassani R, Herkani A, Nouri H, Boukind S, Tassi N, Raji A.
Rev Stomatol Chir Maxillofac. 2011;112(5):313-5.
Trismus Facial palsy
Adult Differential Diagnosis Homo sapiens Male Tetanus Trismus
3
(43.9%)		 20040354
 Tetanus as a cause of rhabdomyolysis and acute renal failure.
Weiss MF, Badalamenti J, Fish E.
Clin Nephrol. 2010;73(1):64-7.
Trismus Risus sardonicus
Accidental Falls Aged, 80 and over Creatine Kinase Disease Progression Fatal Outcome Females Homo sapiens Myoglobin Rhabdomyolysis Tetanus Time Factors
3
(43.9%)		 19918553
(2769323)
 Titration of high dose sedation is effective in severe tetanus: a case report.
Chun P, Ying-Zi H, Yi Y, Hai-Bo Q.
Cases J. 2009;2:6865.
Trismus Risus sardonicus
3
(43.9%)		 19697889
 [Dysfunction of multiple cranial nerves in cephalic tetanus--case report].
Fujii M, Hokari M, Yokoyama A, Miyashita H, Ishihara A, Fujikawa T.
Brain Nerve. 2009;61(8):983-7.
Trismus Facial palsy
Accidental Falls Anti-Bacterial Agents Debridement Homo sapiens Horner Syndrome Male Tetanus Tetanus Antitoxin
3
(43.9%)		 18173031
 Cephalic tetanus with left infranuclear facial palsy.
Sharma VK, Dubey TN, Nayak R, Agarwal A.
J Assoc Physicians India. 2007;55:735-6.
Trismus Facial palsy
RAN
Child Cranial Nerves Homo sapiens Male Tetanus Trismus
3
(43.9%)		 15269587
 Tetanus and the plastic surgeon.
Culbertson TA, Kalliainen LK, Buchele BA.
Ann Plast Surg. 2004;53(2):162-5.
Trismus Risus sardonicus
Accidental Falls Adult Burns, Electric Debridement Homo sapiens Male Respiration, Artificial Tetanus
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 162

HPO ID Term # of case reports
HP:0000211 Trismus 40
HP:0012115 Hepatitis 25
HP:0002063 Rigidity 17
HP:0002015 Dysphagia 14
HP:0003394 Muscle spasm 14
HP:0001250 Seizures 10
HP:0002179 Opisthotonus 10
HP:0003470 Paralysis 10
HP:0025615 Abscess 6
HP:0040212 Risus sardonicus 6
HP:0002878 Respiratory failure 5
HP:0100614 Myositis 5
HP:0000508 Ptosis 4
HP:0000752 Hyperactivity 4
HP:0000822 Hypertension 4
HP:0001945 Fever 4
HP:0002090 Pneumonia 4
HP:0010628 Facial palsy 4
HP:0100658 Cellulitis 4
HP:0100806 Sepsis 4
HP:0000388 Otitis media 3
HP:0001281 Tetany 3
HP:0001482 Subcutaneous nodule 3
HP:0001649 Tachycardia 3
HP:0001888 Lymphopenia 3
HP:0002093 Respiratory insufficiency 3
HP:0002315 Headache 3
HP:0009830 Peripheral neuropathy 3
HP:0012486 Myelitis 3
HP:0012819 Myocarditis 3
HP:0031179 Nuchal rigidity 3
HP:0040264 Jaw pain 3
HP:0100790 Hernia 3
HP:0000969 Edema 2
HP:0001254 Lethargy 2
HP:0001287 Meningitis 2
HP:0001324 Muscle weakness 2
HP:0001332 Dystonia 2
HP:0001695 Cardiac arrest 2
HP:0001873 Thrombocytopenia 2
HP:0001878 Hemolytic anemia 2
HP:0001880 Eosinophilia 2
HP:0002013 Vomiting 2
HP:0002027 Abdominal pain 2
HP:0002094 Dyspnea 2
HP:0002321 Vertigo 2
HP:0002445 Tetraplegia 2
HP:0002595 Ileus 2
HP:0003201 Rhabdomyolysis 2
HP:0003326 Myalgia 2
HP:0006846 Acute encephalopathy 2
HP:0010783 Erythema 2
HP:0012385 Camptodactyly 2
HP:0031925 Rosette 2
HP:0032252 Granuloma 2
HP:0100653 Optic neuritis 2
HP:0100758 Gangrene 2
HP:0000206 Glossitis 1
HP:0000463 Anteverted nares 1
HP:0000473 Torticollis 1
HP:0000563 Keratoconus 1
HP:0000577 Exotropia 1
HP:0000597 Ophthalmoparesis 1
HP:0000602 Ophthalmoplegia 1
HP:0000605 Supranuclear gaze palsy 1
HP:0000622 Blurred vision 1
HP:0000712 Emotional lability 1
HP:0000819 Diabetes mellitus 1
HP:0000836 Hyperthyroidism 1
HP:0000979 Purpura 1
HP:0000989 Pruritus 1
HP:0000999 Pyoderma 1
HP:0001025 Urticaria 1
HP:0001055 Erysipelas 1
HP:0001251 Ataxia 1
HP:0001257 Spasticity 1
HP:0001258 Spastic paraplegia 1
HP:0001260 Dysarthria 1
HP:0001271 Polyneuropathy 1
HP:0001276 Hypertonia 1
HP:0001297 Stroke 1
HP:0001336 Myoclonus 1
HP:0001337 Tremor 1
HP:0001369 Arthritis 1
HP:0001370 Rheumatoid arthritis 1
HP:0001511 Intrauterine growth retardation 1
HP:0001643 Patent ductus arteriosus 1
HP:0001662 Bradycardia 1
HP:0001700 Myocardial necrosis 1
HP:0001788 Premature rupture of membranes 1
HP:0001824 Weight loss 1
HP:0001919 Acute kidney injury 1
HP:0001942 Metabolic acidosis 1
HP:0001943 Hypoglycemia 1
HP:0001974 Leukocytosis 1
HP:0002014 Diarrhea 1
HP:0002018 Nausea 1
HP:0002020 Gastroesophageal reflux 1
HP:0002196 Myelopathy 1
HP:0002204 Pulmonary embolism 1
HP:0002266 Focal clonic seizures 1
HP:0002301 Hemiplegia 1
HP:0002355 Difficulty walking 1
HP:0002510 Spastic tetraplegia 1
HP:0002516 Increased intracranial pressure 1
HP:0002527 Falls 1
HP:0002583 Colitis 1
HP:0002615 Hypotension 1
HP:0002716 Lymphadenopathy 1
HP:0002721 Immunodeficiency 1
HP:0002754 Osteomyelitis 1
HP:0002758 Osteoarthritis 1
HP:0002835 Aspiration 1
HP:0002840 Lymphadenitis 1
HP:0002901 Hypocalcemia 1
HP:0002902 Hyponatremia 1
HP:0002953 Vertebral compression fractures 1
HP:0002965 Cutaneous anergy 1
HP:0003128 Lactic acidosis 1
HP:0003198 Myopathy 1
HP:0003228 Hypernatremia 1
HP:0003323 Progressive muscle weakness 1
HP:0003419 Low back pain 1
HP:0003701 Proximal muscle weakness 1
HP:0004305 Involuntary movements 1
HP:0005214 Intestinal obstruction 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0005943 Respiratory arrest 1
HP:0006965 Acute necrotizing encephalopathy 1
HP:0007460 Autoamputation of digits 1
HP:0007626 Mandibular osteomyelitis 1
HP:0008200 Primary hyperparathyroidism 1
HP:0009900 Unilateral deafness 1
HP:0010553 Oculogyric crisis 1
HP:0011675 Arrhythmia 1
HP:0011897 Neutrophilia 1
HP:0011951 Aspiration pneumonia 1
HP:0012219 Erythema nodosum 1
HP:0012251 ST segment elevation 1
HP:0012393 Allergy 1
HP:0012399 Pressure ulcer 1
HP:0012531 Pain 1
HP:0012532 Chronic pain 1
HP:0012799 Unilateral facial palsy 1
HP:0025406 Asthenia 1
HP:0025430 High-pitched cry 1
HP:0030351 Urticarial plaque 1
HP:0030834 Shoulder pain 1
HP:0031002 Neuritis 1
HP:0031013 Ankylosis 1
HP:0031180 Erythema migrans 1
HP:0031218 Inappropriate antidiuretic hormone secretion 1
HP:0031273 Shock 1
HP:0031281 Sialadenitis 1
HP:0031625 Pseudoaneurysm 1
HP:0031670 Continuous heart murmur 1
HP:0032044 Decreased vigilance 1
HP:0100550 Tendon rupture 1
HP:0100601 Eclampsia 1
HP:0100665 Angioedema 1
HP:0100729 Large face 1
HP:0100774 Hyperostosis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID