Sandbox kiran3: Difference between revisions
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[[Adrenoleukodystrophy]], | [[Adrenoleukodystrophy]], | ||
[[Behcet's syndrome]], | [[Behcet's syndrome]], | ||
[[Chromosome 1p36 deletion syndrome]] | [[Chromosome 1, 1p36 deletion syndrome|Chromosome 1p36 deletion syndrome]] | ||
[[Chromosome 22 | [[Chromosome 22 (human)|Chromosome 22 ring]], | ||
[[Chromosome 22 trisomy | [[Trisomy 22|Chromosome 22 trisomy mosaic]], | ||
[[Connective tissue disease (overlap syndrome)]], | [[Connective tissue disease (overlap syndrome)]], | ||
[[Emanuel syndrome ]], | [[Emanuel syndrome ]], | ||
Revision as of 18:59, 17 December 2015
- 10th cranial nerve disorder
- Aberrant subclavian artery
- Abscess
- Achalasia
- Achalasia cardia
- Achalasia, familial esophageal
- Achalasia-addisonian syndrome
- Achromatopsia
- Acoustic neuroma
- Adrenoleukodystrophy
- Aerophagia
- Agranulocytosis
- Alcoholism
- Allergic swelling
- Amyloidosis
- Amyotrophic lateral sclerosis
- Angina tonsillaris
- Anxiety disorders
- Aortic aneurysm
- Arizona bark scorpion poisoning
- Arnold-chiari malformation type 3
- Artemether and lumefantrin
- Aspiration of foreign body
- Autonomic nerve disorders
- Autonomic neuropathy
- Autosomal recessive spastic paraplegia, type 11
- Avellis syndrome
- Babinski–Nageotte syndrome
- Barret's syndrome
- Basal ganglia disease
- Basilar artery insufficiency syndrome
- Behcet's syndrome
- Benign tumors
- Botulinum toxin
- Botulism
- Brainstem stroke
- Brain stem tumor
- Bronchial carcinoma
- Bulbar palsy
- Calcinosis-raynaud's sclerodactyly-telangiectasia syndrome
- Candida esophagitis
- Candidiasis
- Canomad syndrome
- Carcinoma of the vocal tract
- Carotid body tumor
- Carotid paraganglioma
- Cascade stomach
- Caustic esophagitis
- Central pontine myelinosis
- Central vagal nucleus lesion
- Central hypoglossal nerve paralysis
- Cerebellar stroke
- Cerebral palsy
- Cerebrovascular accident
- Cervical osteophytes
- Chagas disease
- Charge syndrome
- Chemical burns
- Chemotherapy
- Chordoma
- Chromosome 1p36 deletion syndrome
- Chromosome 22 ring
- Chromosome 22 trisomy mosaic
- Cobra poisoning
- Congenital bronchogenic cyst
- Connective tissue disease
- Crest syndrome
- Cricopharyngeal spasm
- Crisponi syndrome
- Crohn's disease of the esophagus
- Cushing's syndrome
- Cyclosporine toxicity
- Cytarabine
- Cytomegalovirus
- Cytoplasmic body myopathy
- Dementia
- Dermatomyositis
- Diabetic neuropathy
- Diffuse esophageal spasm
- Diffuse idiopathic skeletal hyperostosis
- Diffuse esophageal spasm
- Diffuse systemic sclerosis
- Diphtheria
- Distal myopathy 2
- Diverticula
- Diverticulum
- Double aortic arch
- Dystonia
- Eagle syndrome
- Elongated styloid process
- Emanuel syndrome
- Enlarged aorta
- Enlarged left atrium
- Eosinophilic esophagitis
- Eosinophilic gastroenteritis
- Epiglottitis
- Epileptic encephalopathy, early infantile, 1
- Esophageal achalasia
- Esophageal atresia
- Esophageal cancer
- Esophageal cyst
- Esophageal diverticulum
- Esophageal leiomyoma
- Esophageal obstruction by a foreign body
- Esophageal pouch
- Esophageal spasm
- Esophageal stricture
- Esophageal web
- Esophageal crohn's disease
- Esophageal moniliasis
- Esophageal sarcoidosis
- Esophageal trauma
- Esophagitis
- Esophagotracheal fistula
- External esophageal compression
- Extreme spinal curvature
- Fluoridated toothpaste
- Food bolus
- Facial Onset Sensory Motor Neuropathy syndrome
- Franek-bocker-kahlen syndrome
- Frontotemporal dementia
- Functional disorders
- Gastric cancer
- Gastric volvulus
- Gastritis
- Gastroesophageal reflux
- Gastroparesis
- Gaucher disease
- Gaucher disease type 2
- Global hystericus
- Globus syndrome
- Goiter
- Graft-versus-host disease
- Guillain-Barré syndrome
- Head trauma
- Herpangina
- Herpes simplex virus
- Hiatal hernia
- Huntington disease
- Huntington's chorea
- Hydroxocobalamin
- Hyperthyroidism
- Hypokalemia
- Hypomagnesemia primary
- Hypophosphatemia
- Hypothyroidism
- Idiopathic human immunodeficiency virus ulcers
- Impaired sensitivity in the larynx
- Inclusion body myositis
- Infantile striato-thalamic degeneration
- Infectious esophagitis
- Intramural pseudodiverticulosis
- Ixabepilone
- Laryngeal cancer
- Laryngeal papillomatosis
- Lateral funiculus angina
- Lead poisoning
- Leiomyoma
- Lhermitte-cornil-quesnel syndrome
- Lissencephaly, type 1, x-linked
- Ludwig's angina
- Lyme disease
- Lymph granulomatosis
- Lymphadenopathy
- Lymphocytic esophagitis
- Malignancy
- Malignant lung cancer
- Mass brain lesion
- Mediastinal mass
- Mediastinitis
- Metabolic encephalopathies
- Microcephaly brain defect spasticity hypernatremia
- Mitochondrial neurogastrointestinal encephalopathy syndrome
- Mitral valve stenosis
- Mononucleosis
- Motor neuron disease
- Mucositis
- Multiple sclerosis
- Multiple system atrophy
- Mumps
- Muscular dystrophy, Duchenne and Becker type
- Myasthenia gravis
- Congenital myasthenic syndrome
- Myoneurogastrointestinal encephalopathy syndrome
- Myopathy
- Myotonic dystrophy
- Nasopharyngeal carcinoma
- Neck cancer
- Nemaline myopathy 1
- Neonatal tetanus
- Neuroferritinopathy
- Neuroleptics
- Neurosarcoidosis
- Nutcracker esophagus
- Oculopharyngeal muscular dystrophy
- Odontoma
- Esophageal cancer
- Esophageal foreign body
- esophageal ring
- Esophageal web
- Esophagitis
- Ondine's curse
- Opitz-frias syndrome
- Oral candidiasis
- Oral cavity tumor
- Oral pharyngeal disorders
- Oral submucous fibrosis
- Oropharyngeal cancer
- Osteophytes
- Palate cancer
- Palatoplegia after damage to the vagal nerve or the accessory nerve
- Pallidopyramidal syndrome
- Paracoccidioidomycosis
- Paraganglioma
- Paraneoplastic limbic encephalitis
- Paraneoplastic syndrome
- Parkinson disease
- Peptic esophagitis
- Peptic stricture
- Pergolide
- Pericarditis
- Peripheral neuropathy
- Peripheral tongue paralysis with lesions of the hypoglossal nerve
- Pharyngeal pouch
- Pharyngitis
- Pharynx cancer
- Pierre Robin syndrome
- Pill esophagitis
- Pleuritis
- Plummer-Vinson syndrome
- Polio
- Poliomyelitis
- Polyradiculitis
- Pontocerebellar hypoplasia type 2a
- Post surgery (laryngeal, esophageal, gastric)
- Post polio syndrome
- Postsurgical muscular or neurogenic
- Primary lateral sclerosis, adult
- Primary motility disorders
- Pseudoachalasia
- Pseudoadrenoleukodystrophy
- Pseudobulbar paralysis
- Pyloric stenosis
- Quinsy
- Rabies
- Radiation esophagitis
- Radiation therapy
- Recent tracheotomy
- Reflux esophagitis
- Retropharyngeal abscess
- Rheumatoid arthritis
- Riedel thyroiditis
- Esophageal web
- Riociguat
- Rumination disorder
- Sarcoidosis
- Sargramostim
- Scarlet fever
- Schatzki ring
- Scleroderma
- [Esophageal motility disorder[|Secondary motility disorders]]
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Shy-Drager Syndrome
- Small cell lung cancer
- Spastic paraplegia 11, autosomal recessive
- Spinal muscular atrophy type I
- Spinocerebellar ataxia 17
- Spinocerebellar ataxia 22
- Spinocerebellar ataxia, autosomal recessive 1
- Stevens-Johnson syndrome
- Stomach cancer
- Stomatitis
- Striatonigral degeneration infantile
- Stroke
- Stuve-wiedemann dysplasia
- Subacute granulomatous thyroiditis
- Subacute thyroiditis
- Supraglottic laryngeal cancer
- Syphilis
- Syringobulbia
- Systemic lupus erythematosus
- Systemic sclerosis
- Tardive dyskinesia
- Tetanus
- Throat cancer
- Thyroglossal tract cyst
- Thyroid cancer, anaplastic
- Thyrotoxicosis
- Tiagabine
- Tongue cancer
- Tongue conditions
- Tonsil cancer
- Tonsil disorders
- Tonsillar cancer
- Tonsillar abscess
- Typhoid fever angina
- Ulcer
- Upper oesophageal sphincter dysfunction
- Vagal paraganglioma
- Vascular abnormality
- Vascular ring with right aortic arch
- Vincent's angina
- Wallenberg's syndrome
- Wiedemann–Rautenstrauch syndrome
- Wilson disease
- Zenker's diverticulum
Aberrant subclavian artery,
Achalasia-addisonian syndrome,
Achromatopsia,
Adrenoleukodystrophy,
Behcet's syndrome,
Chromosome 1p36 deletion syndrome
Chromosome 22 ring,
Chromosome 22 trisomy mosaic,
Connective tissue disease (overlap syndrome),
Emanuel syndrome ,
Extreme spinal curvature,
Gaucher disease,
Huntington disease,
Huntington's chorea,
Lissencephaly, type 1, x-linked ,
Muscular dystrophy, duchenne and becker type ,
Myotonic dystrophy,
Nemaline myopathy 1 ,
Oculopharyngeal muscular dystrophy,
Pseudoadrenoleukodystrophy ,
Spinal muscular atrophy type I,
Spinocerebellar ataxia 17 ,
Spinocerebellar ataxia 22 ,
Spinocerebellar ataxia, autosomal recessive 1 ,
Stuve-wiedemann dysplasia,
Vascular ring with right aortic arch,
Wiedemann-rautenstrauch syndrome,
Wilson disease,
Oropharyngeal cancer, Ortner's syndrome, palate cancer, palatine tonsil,
post surgery (laryngeal, esophageal, gastric), presbyphagia, pseudoachalasia, quinsy, radiation esophagitis/stricture, retropharyngeal abscess, Schatzki ring, scleroderma, Wilson disease, Zenker's diverticulum