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• Conditions (70): Achalasia, Genetic and Rare Conditions, Digestive and Gastrointestinal, and 67 others Achalasia, Genetic and Rare Conditions, Digestive and Gastrointestinal, Esophageal Dysphagia, Hirschsprung's Disease, Eosinophilic Gastroenteritis, Fructose Intolerance, Diseases and Conditions, CREST Syndrome, PANDA Syndrome, Agenesis of Corpus Callosum, Trimethylaminuria, Anencephaly, Addison's Disease, Dercum's Disease, Dandy Walker Syndrome, Fragile X Syndrome, Pachygyria, 1p36 Deletion Syndrome, Aarskog Syndrome, Legg-Calve-Perthes Disease, Ledderhose Disease, Darier's Disease, Behcet's Syndrome, Empty Sella Syndrome, Cri-du-Chat Syndrome, Cleidocranial Dysplasia, Kartagener Syndrome, Sjogren's Syndrome, Marfan syndrome, Menkes Kinky Hair Syndrome, Androgen Insensitivity Syndrome, Adie Syndrome, Angelman syndrome, Cushings Syndrome, Williams Syndrome, Hydrocephalus, Factor V Leiden, Simpson-Golabi-Behmel Syndrome, Friedreich's Ataxia, Inflammatory Linear Verrucous Epidermal Nevus, Ehlers-Danlos syndrome, Adrenal Insufficiency, Hashimoto's Encephalopathy, Acute Intermittent Porphyria, 9p Minus, Post-Polio Syndrome, Idiopathic Edema, Lissencephaly, Pallister-Hall syndrome, Epidermal Nevus, Cerebral Palsy, Complete Androgen Insensitivity Syndrome, Arnold-Chiari Malformation, Evan's Syndrome, Acromegaly, Cystic Fibrosis, Autism / Autism Spectrum, Esophageal Atresia , Achondroplastic Dwarfism, Elephantiasis, Langerhans Cell Histiocytosis, Klinefelter's Syndrome, Asperger's Syndrome, Susac syndrome, Hailey-Hailey disease, Beal's syndrome, Sturge-Weber syndrome, Ellis-van Creveld syndrome, Spina Bifida [hide]
• Groups (26): Hirschsprung's Disease, Short Bowel Syndrome, Esophageal Atresia and/or Tracheosophageal Fistula, and 23 others Hirschsprung's Disease, Short Bowel Syndrome, Esophageal Atresia and/or Tracheosophageal Fistula, Eosinophilic Gastroenteritis, Primary Sclerosing Cholangitis, Rare 'Orphan' Disorders, PANDAS Syndrome, Agenesis of Corpus Callosum, Trimethylaminuria, Dercum's Disease, Addison's Disease, Anencephaly, Blepharophimosis, Dandy Walker Syndrome, Pachygyria, Ledderhose Disease, Fragile X Syndrome, Aarskog Syndrome, Microphthalmia, Legg-Calve-Perthes Disease, Darier's Disease, Cri-du-Chat Syndrome, 1p36 Deletion Syndrome, Empty Sella Syndrome, Behcet's Syndrome, Cleidocranial Dysplasia [hide]
• Symptoms (9): Blepharophimosis, Sweet Syndrome, Club Foot, and 6 others Blepharophimosis, Sweet Syndrome, Club Foot, Von Willebrand disease, Scleroderma, Castleman's Disease, pyoderma gangrenosum, Tetralogy of Fallot, Achalasia [hide]
• Treatments (49): Heller's myotomy for achalasia, Pneumatic dilatation for achalasia, Esophageal Dilatation, and 46 others Heller's myotomy for achalasia, Pneumatic dilatation for achalasia, Esophageal Dilatation, Botulinum Toxin, Heller Myotomy, Procedures, Benzatropine Methanesulfonate, Trihexyphenidyl Hydrochloride, Alendronate 35 MG Oral Tablet, Alendronate 5 MG Oral Tablet, Benztropine 1 MG Oral Tablet, Alendronate 35 MG, Trihexyphenidyl 2 MG Oral Tablet, Benztropine 1 MG/ML Injectable Solution, Alendronate, risedronate sodium, BENZTROPINE MESYLATE 1 MG, Alendronate 40 MG Oral Tablet, Risedronate 30 MG Oral Tablet, Pneumatic dilatation for achalasia, Alendronate 10 MG, RISEDRONATE SODIUM 35 MG, TRIHEXYPHENIDYL HYDROCHLORIDE 2 MG/5ML, BENZTROPINE MESYLATE 2 MG, Trihexyphenidyl, Risedronate, Risedronate 5 MG Oral Tablet, Risedronate 35 MG Oral Tablet, Alendronate 5 MG, FLAVOXATE HYDROCHLORIDE 100 MG, BENZTROPINE MESYLATE 0.5 MG, Alendronate 40 MG, Flavoxate Hydrochloride, Benztropine 0.5 MG Oral Tablet, Trihexyphenidyl 5 MG Oral Tablet, Alendronate 70 MG Oral Tablet, Trihexyphenidyl 0.4 MG/ML Elixir, Alendronate 70 MG, Risedronate 30 MG, TRIHEXYPHENIDYL HYDROCHLORIDE 2 MG, Benztropine, Alendronate 10 MG Oral Tablet, Flavoxate 100 MG Oral Tablet, Trihexyphenidyl 5 MG Extended Release Capsule, risedronic acid 5 MG, TRIHEXYPHENIDYL HYDROCHLORIDE 5 MG, BENZTROPINE MESYLATE 1 MG/ML, Flavoxate, Benztropine 2 MG Oral Tablet [hide]

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