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• Conditions (37): Genetic and Rare Conditions, Achalasia, Agenesis of Corpus Callosum, and 34 others Genetic and Rare Conditions, Achalasia, Agenesis of Corpus Callosum, Hirschsprung's Disease, Trimethylaminuria, Addison's Disease, Anencephaly, Dercum's Disease, Fragile X Syndrome, Dandy Walker Syndrome, 1p36 Deletion Syndrome, Aarskog Syndrome, Pachygyria, Legg-Calve-Perthes Disease, Behcet's Syndrome, PANDA Syndrome, Cri-du-Chat Syndrome, Ledderhose Disease, Darier's Disease, Empty Sella Syndrome, Cleidocranial Dysplasia, Fructose Intolerance, Kartagener Syndrome, Adie Syndrome, Androgen Insensitivity Syndrome, Menkes Kinky Hair Syndrome, Sjogren's Syndrome, Marfan syndrome, Factor V Leiden, Eosinophilic Gastroenteritis, Williams Syndrome, Simpson-Golabi-Behmel Syndrome, Friedreich's Ataxia, Hashimoto's Encephalopathy, Angelman syndrome, Post-Polio Syndrome, Cerebral Palsy [hide]
• Groups (26): Achalasia, Rare 'Orphan' Disorders, Hirschsprung's Disease, and 23 others Achalasia, Rare 'Orphan' Disorders, Hirschsprung's Disease, PANDAS Syndrome, Trimethylaminuria, Agenesis of Corpus Callosum, Dercum's Disease, Addison's Disease, Blepharophimosis, Anencephaly, Dandy Walker Syndrome, Fragile X Syndrome, Pachygyria, Ledderhose Disease, Aarskog Syndrome, Legg-Calve-Perthes Disease, Microphthalmia, Cri-du-Chat Syndrome, Darier's Disease, Behcet's Syndrome, Empty Sella Syndrome, Cleidocranial Dysplasia, 1p36 Deletion Syndrome, Fructose Intolerance, Kartagener Syndrome, Cushing's Syndrome [hide]
• Symptoms (8): Blepharophimosis, Sweet Syndrome, Club Foot, and 5 others Blepharophimosis, Sweet Syndrome, Club Foot, Von Willebrand disease, Castleman's Disease, Scleroderma, pyoderma gangrenosum, Tetralogy of Fallot [hide]

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