Genetic disease

cyclic vomiting syndrome Tourette syndrome Fukuyama congenital muscular dystrophy accessory navicular bone Severe X-linked intellectual disability, Gustavson type specific phobia Obesity hypoventilation syndrome uterine malformation aspirin-exacerbated respiratory disease Imperforate hymen apparent mineralocorticoid excess syndrome trigger finger disorder ainhum tooth ankylosis Marshall–Smith syndrome Perry syndrome gastroesophageal reflux disease Schimke immuno-osseous dysplasia Schimke immuno-osseous dysplasia Warsaw breakage syndrome Duplicated ureter prune belly syndrome Genetics of infertility Apraxia of Lid Opening Finnish heritage disease du Pan syndrome Mowat-Wilson syndrome Tone deafness galactorrhea NGLY1-deficiency Alcohol intolerance animal genetic disease protein-losing enteropathy Hemochromatosis type 4 failure of eruption of teeth familial isolated deficiency of vitamin E pulmonary atresia with Ventricular Septal Defect Microcephaly with spastic diplegia Microcephaly with spastic diplegia Thomas syndrome rigid spine syndrome Sorsby's fundus dystrophy familial eosinophilia pyruvate kinase deficiency purine nucleoside phosphorylase deficiency enterocolitis motion sickness enhanced S-cone syndrome aromatic L-amino acid decarboxylase deficiency primary congenital glaucoma