| Goods and Services | Pharmaceutical preparations for the treatment of infectious diseases; pharmaceutical preparations for the treatment of non-infectious diseases, namely immunological diseases, autoimmune diseases, cardiovascular diseases, inflammatory diseases, and neurodegenerative diseases; pharmaceutical preparations for treating respiratory diseases and asthma; pharmaceutical preparations for treatment of pulmonary diseases; pharmaceutical preparations for the treatment of hypertension; pharmaceutical preparations for use in the treatment of cancer; pharmaceutical preparations for use in chemotherapy; pharmaceutical preparations for rare diseases, namely ACTH Deficiency; AIDS (Acquired Immune Deficiency Syndrome); AIDS Dysmorphic Syndrome; APECED Syndrome; Aarskog Syndrome; Aase Syndrome; Abetalipoproteinemia; Ablepharon Macrostomia Syndrome; Acanthocheilonemiasis; Acanthocytosis; Acanthosis Nigricans; Achalasia; Achard Thiers Syndrome; Achondrogenesis; Achondroplasia ; Acidemia, Isovaleric; Acidemia, Methylmalonic; Acidemia, Propionic; Acne Rosacea; Acoustic Neuroma; Acquired Aplastic Anemia; Acrocallosal Syndrome, Schinzel Type; Acrodermatitis Enteropathica; Acrodysostosis; Acromegaly; Acromesomelic Dysplasia; Acromicric Dysplasia; Acute Respiratory Distress Syndrome; Adams Oliver Syndrome; Addison's Disease; Adenoid Cystic Carcinoma; Adenylosuccinate Lyase Deficiency; Adie Syndrome; Adrenal Hyperplasia, Congenital (General); Adrenoleukodystrophy; Afibrinogenemia, Congenital; Agammaglobulinemias, Primary; Agenesis of Corpus Callosum; Agnosia, Primary Visual; Agranulocytosis, Acquired; Ahumada-Del Castillo Syndrome; Aicardi Syndrome; Alagille Syndrome; Albinism; Alexander Disease; Alkaptonuria; Allan Herndon Syndrome; Alopecia Areata; Alpers Disease; Alpha-1-Antitrypsin Deficiency; Alpha-Mannosidosis; Alport Syndrome; Alstrom Syndrome; Alternating Hemiplegia of Childhood; Alveolar Capillary Dysplasia; Alveolar Soft Part Sarcoma; Alveolitis, Extrinsic Allergic; Alzheimer's Disease; Ameloblastoma; Amelogenesis Imperfecta; Amenorrhea, Primary; Amenorrhea-Galactorrhea Syndrome; Amniotic Bands; Amyloidosis; Amyotrophic Lateral Sclerosis; Anaphylaxis; Andersen Disease (GSD IV); Androgen Insensitivity Syndrome, Partial; Anemia, Blackfan Diamond; Anemia, Fanconi's; Anemia, Hemolytic, Acquired Autoimmune; Anemia, Hemolytic, Cold Antibody; Anemia, Hemolytic, Warm Antibody; Anemia, Hereditary Nonspherocytic Hemolytic; Anemia, Hereditary Spherocytic Hemolytic; Anemia, Megaloblastic; Anemia, Pernicious; Anemias, Sideroblastic ; Anencephaly; Angelman Syndrome; Angioedema, Hereditary; Aniridia; Aniridia Cerebellar Ataxia Mental Deficiency; Ankylosing Spondylitis; Anodontia; Anorexia Nervosa; Anthrax; Antiphospholipid Syndrome; Antisocial Personality Disorder; Antithrombin III Deficiency; Antley Bixler Syndrome; Apert Syndrome; Aplasia Cutis Congenita; Apnea, Infantile; Apnea, Sleep; Apraxia; Arachnoid Cysts; Arachnoiditis; Arginase Deficiency; Argininosuccinic Aciduria; Arnold-Chiari Malformation; Arteriovenous Malformation; Arteritis, Giant Cell; Arteritis, Takayasu; Arthritis, Infectious; Arthritis, Juvenile Rheumatoid; Arthritis, Psoriatic; Arthrogryposis Multiplex Congenita; Asherman's Syndrome; Aspartylglycosaminuria; Asperger's Syndrome; Aspergillosis; Astrocytoma; Astrocytoma, Malignant; Ataxia Telangiectasia; Ataxia with Vitamin E Deficiency; Ataxia, Friedreich's; Ataxia, Hereditary, Autosomal Dominant; Atrial Septal Defects; Atrioventricular Septal Defect; Attention Deficit Hyperactivity Disorder; Atypical Hemolytic Uremic Syndrome; Atypical Mole Syndrome; Autism; Autoimmune Polyendocrine Syndrome Type II; Autoimmune Thyroiditis; Babesiosis; Balantidiasis; Baller Gerold Syndrome; Balo Disease; Bannayan Riley Ruvalcaba Syndrome; Banti's Syndrome; Bardet Biedl Syndrome; Barrett Esophagus; Barth Syndrome; Bartonellosis; Bartter's Syndrome; Batten Disease; Beals Syndrome; Beckwith Wiedemann Syndrome; Behcet's Syndrome; Bejel; Bell's Palsy; Benign Essential Tremor; Bernard Soulier Syndrome; Berylliosis; Best Vitelliform Macular Dystrophy; Biliary Atresia, Extrahepatic; Binswanger's Disease; Bjornstad Syndrome; Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex; Blastomycosis; Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome; Blepharospasm, Benign Essential; Bloom Syndrome; Blue Diaper Syndrome; Blue Rubber Bleb Nevus; Borjeson Syndrome; Botulism; Bowen Hutterite Syndrome; Bowen's Disease; Bowenoid Papulosis; Brachial Plexus Palsy; Brain Tumors, General; Branchio Oculo Facial Syndrome; Branchio Oto Renal Syndrome; Bronchopulmonary Dysplasia (BPD); Brown Sequard Syndrome; Brown Syndrome; Brucellosis; Bubonic Plague; Budd Chiari Syndrome; Buerger's Disease; Bulimia; Bullous Pemphigoid; Burning Mouth Syndrome; C Syndrome; CHARGE Syndrome; Campomelic Syndrome; Camurati-Engelmann Disease; Canavan Disease; Cancer, Colon; Cancer, Prostate; Cancers, Skin, General; Candidiasis; Carbamyl Phosphate Synthetase Deficiency; Carbohydrate Deficient Glycoprotein Syndrome Type Ia ; Carboxylase Deficiency, Multiple; Carcinoid Syndrome; Carcinoma, Renal Cell; Carcinoma, Squamous Cell; Cardiofaciocutaneous Syndrome; Carnitine Deficiency Syndromes; Carnitine Palmitoyltransferase Deficiency; Carnosinemia; Caroli Disease; Carpal Tunnel Syndrome; Carpenter Syndrome; Castleman's Disease; Cat Eye Syndrome; Cat Scratch Disease; Cataract Dental Syndrome; Cataracts; Catel Manzke Syndrome; Caudal Regression Syndrome;Cavernous Malformation; Cayler Syndrome; Celiac Disease; Central Core Disease; Central Hypoventilation Syndrome, Congenital; Cerebellar Agenesis; Cerebellar Degeneration, Subacute; Cerebral Palsy; Cerebro Oculo Facio Skeletal Syndrome; Cerebrocostomandibular Syndrome; Chagas Disease; Chalazion; Chandler's Syndrome; Charcot Marie Tooth Disease; Chediak Higashi Syndrome; Chiari Frommel Syndrome; Chikungunya; Chlamydia; Cholangitis, Primary Sclerosing; Cholecystitis; Cholera; Cholestasis; Chondrocalcinosis, Familial Articular; Chordoma; Chorea, Sydenham's; Choroideremia; Choroiditis, Serpiginous; Chromosome 10, Distal Trisomy 10q ; Chromosome 10, Monosomy 10p; Chromosome 11, Partial Monosomy 11q; Chromosome 11, Partial Trisomy 11q; Chromosome 13, Partial Monosomy 13q; Chromosome 14 Ring; Chromosome 14, Trisomy Mosaic; Chromosome 15 Ring; Chromosome 15, Distal Trisomy 15q; Chromosome 18 Ring; Chromosome 18, Monosomy 18p; Chromosome 18, Tetrasomy 18p; Chromosome 18q- Syndrome; Chromosome 21 Ring; Chromosome 22 Ring; Chromosome 22, Trisomy Mosaic; Chromosome 3, Monosomy 3p2; Chromosome 3, Trisomy 3q2; Chromosome 4 Ring; Chromosome 4, Monosomy 4q; Chromosome 4, Monosomy Distal 4q; Chromosome 4, Partial Trisomy Distal 4q; Chromosome 4, Trisomy 4p; Chromosome 5, Trisomy 5p; Chromosome 6 Ring; Chromosome 6, Partial Trisomy 6q; Chromosome 7, Partial Monosomy 7p; Chromosome 8, Monosomy 8p2; Chromosome 9 Ring; Chromosome 9, Partial Monosomy 9p; Chromosome 9, Tetrasomy 9p; Chromosome 9, Trisomy 9p (Multiple Variants); Chromosome 9, Trisomy Mosaic; Chronic Fatigue Syndrome; Chronic Fatigue Syndrome/Myalgic Encephalomyelitis; Chronic Inflammatory Demyelinating Polyneuropathy; Churg Strauss Syndrome; Ciguatera Fish Poisoning; Cirrhosis, Primary Biliary; Citrullinemia; Cleft Palate and Cleft Lip; Cleidocranial Dysplasia; Clubfoot; Coats' Disease; Cochin Jewish Disorder; Cockayne Syndrome; Coffin Lowry Syndrome; Coffin Siris Syndrome; Cogan Reese Syndrome; Cohen Syndrome; Colitis, Collagenous; Colitis, Ulcerative; Colorado Tick Fever; Common Variable Immunodeficiency; Condyloma; Cone Dystrophy; Congenital Fibrosis of the Extraocular Muscles; Congenital Varicella Syndrome; Conjunctivitis, Ligneous; Conn Syndrome; Conradi Hunermann Syndrome; Conversion Disorder; Cor Triatriatum; Corneal Dystrophies; Cornelia de Lange Syndrome; Corticobasal Degeneration; Costello Syndrome; Cowpox; Craniofrontonasal Dysplasia; Craniometaphyseal Dysplasia; Craniosynostosis, Primary; Creutzfeldt Jakob Disease; Cri du Chat Syndrome; Crigler Najjar Syndrome Type I; Crohn's Disease; Cronkhite-Canada Syndrome; Crouzon Syndrome; Cryoglobulinemia, Essential Mixed; Cryptococcosis; Cushing's Syndrome; Cutaneous T-Cell Lymphomas; Cutis Laxa; Cutis Marmorata Telangiectatica Congenita; Cyclic Vomiting Syndrome; Cystic Fibrosis; Cystic Hygroma; Cysticercosis; Cystinosis; Cystinuria; Cytochrome C Oxidase Deficiency; Cytomegalovirus Infection; DOOR Syndrome; Dandy Walker Malformation; De Barsy Syndrome; De Santis Cacchione Syndrome; Degos Disease; Dejerine Sottas Disease; Dengue Fever; Dentin Dysplasia, Coronal; Dentin Dysplasia, Type I; Dentinogenesis Imperfecta Type III; Depersonalization Disorder; Dercum Disease; Dermatitis Herpetiformis; Dermatitis, Atopic; Dermatitis, Contact; Dermatomyositis; Devic Disease; Dextrocardia with Situs Inversus; DiGeorge Syndrome; Diabetes Insipidus; Diabetes, Insulin Dependent; Diastrophic Dysplasia; Diencephalic Syndrome; Diffuse Idiopathic Skeletal Hyperostosis; Dilatation of the Pulmonary Artery, Idiopathic; Disaccharide Intolerance I; Diverticulitis; Diverticulosis; Down Syndrome; Dracunculosis; Drash Syndrome; Duane Syndrome; Dubin Johnson Syndrome; Dubowitz Syndrome; Duodenal Atresia or Stenosis; Dupuytren's Contracture; Dyggve Melchior Clausen Syndrome; Dysautonomia, Familial; Dyschondrosteosis; Dyskeratosis Congenita; Dyslexia; Dysplasia, Epiphysealis Hemimelica; Dysplasia, Fibrous; Dysthymia; Dystonia; Dystrophy, Asphyxiating Thoracic; Dystrophy, Myotonic; Eales Disease; Ear, Patella, Short Stature Syndrome; Ectodermal Dysplasias; Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate; Edema, Idiopathic; Ehlers Danlos Syndrome; Eisenmenger Syndrome; Elephantiasis; Ellis Van Creveld Syndrome; Emphysema, Congenital Lobar; Empty Sella Syndrome; Encephalitis, Herpes Simplex; Encephalitis, Japanese; Encephalitis, Rasmussen's; Encephalocele; Endocardial Fibroelastosis; Endocarditis, Infective; Endometriosis; Endomyocardial Fibrosis; Enterobiasis; Eosinophilia Myalgia; Eosinophilic Fasciitis; Epidermal Nevus Syndrome; Epidermolysis Bullosa; Epidermolytic Hyperkeratosis; Epididymitis; Epilepsy; Epitheliopathy, Acute Posterior Multifocal Placoid Pigment; Erdheim Chester Disease; Erysipelas; Erythema Multiforme; Erythroderma desquamativa of Leiner; Erythrokeratodermia with Ataxia; Erythromelalgia; Erythropoietic Protoporphyria; Esophageal Atresia and/or Tracheoesophageal Fistula; Essential Iris Atrophy; Ewing's Sarcoma; Exostoses, Multiple; FG Syndrome; Fabry Disease; Facioscapulohumeral Muscular Dystrophy; Factor IX Deficiency; Factor XIII Deficiency; Fahr's Disease; Familial Adenomatous Polyposis; Familial Eosinophilic Cellulitis; Familial Juvenile Hyperuricemic Nephropathy; Familial Lipoprotein Lipase Deficiency; Farber's Disease; Fascioliasis; Felty Syndrome; Femoral Facial Syndrome; Fetal Alcohol Syndrome; Fetal Hydantoin Syndrome; Fetal Retinoid Syndrome; Fetal Valproate Syndrome; Fiber Type Disproportion, Congenital; Fibrodysplasia Ossificans Progressiva (FOP); Fibromatosis, Congenital Generalized; Fibromyalgia; Filariasis; Filippi Syndrome; Fitz Hugh Curtis Syndrome; Floating Harbor Syndrome; Focal Dermal Hypoplasia; Forbes Disease; Formaldehyde Poisoning; Fountain Syndrome; Fournier Gangrene; Fox Fordyce Disease; Fragile X Syndrome; Fraser Syndrome; Freeman Sheldon Syndrome; Frey's Syndrome; Froelich's Syndrome; Frontofacionasal Dysplasia; Frontonasal Dysplasia; Fructose Intolerance, Hereditary; Fructosuria; Fryns Syndrome; Fukuyama Type Congenital Muscular Dystrophy; Galactosemia; Galloway Mowat Syndrome; Gardner Syndrome; Gastritis, Chronic, Erosive; Gastritis, Giant Hypertrophic; Gastroenteritis, Eosinophilic; Gastroesophageal Reflux; Gastrointestinal Stromal Tumors; Gastroschisis; Gaucher Disease; Gerstmann Syndrome; Gianotti Crosti Syndrome; Giant Cell Myocarditis; Giardiasis; Gilbert Syndrome; Glanzmann Thrombasthenia; Glioblastoma Multiforme; Glucose Galactose Malabsorption; Glucose-6-Phosphate Dehydrogenase Deficiency; Glutaricaciduria I; Glutaricaciduria II; Glycogen Storage Disease Type V; Glycogen Storage Disease VIII; Goldenhar Syndrome (Oculo Auriculo Vertebral Spectrum); Goodman Syndrome; Goodpasture Syndrome; Gordon Syndrome; Gorham's Disease; Gorlin Chaudhry Moss Syndrome; Gottron Syndrome; Graft versus Host Disease; Granuloma Annulare; Granulomatosis, Lymphomatoid; Granulomatous Disease, Chronic; Graves' Disease; Greig Cephalopolysyndactyly Syndrome; Grover's Disease; Growth Delay, Constitutional; Growth Hormone Deficiency; Guillain Barre Syndrome; Hageman Factor Deficiency; Hajdu Cheney Syndrome; Hallermann Streiff syndrome; Hand Foot Mouth Syndrome; Hanhart Syndrome; Hantavirus Pulmonary Syndrome; Hartnup Disease; Hay-Wells Syndrome; Headache, Cluster; Heart Block, Congenital; Heavy Metal Poisoning; Hemangioma Thrombocytopenia Syndrome; Hematuria, Benign, Familial; Hemochromatosis, Hereditary; Hemoglobinuria, Paroxysmal Cold; Hemoglobinuria, Paroxysmal Nocturnal; Hemolytic Uremic Syndrome; Hemophilia; Hemorrhagic Telangiectasia, Hereditary; Hepatic Fibrosis, Congenital; Hepatitis B; Hepatitis C; Hepatitis, Neonatal; Hepatorenal Syndrome; Hermansky Pudlak Syndrome; Hermaphroditism, True; Herpes, Neonatal; Hers Disease; Hiccups, Chronic; Hidradenitis Suppurativa; Hirschsprung's Disease; Histidinemia; Hodgkin's Disease; Holoprosencephaly; Holt Oram Syndrome; Homocystinuria; Horner's Syndrome; Human Granulocytic Ehrlichiosis (HGE); Human Monocytic Ehrlichiosis (HME); Hunter Syndrome; Huntington's Disease; Hydranencephaly; Hydrocephalus; Hyper IgM Syndrome; Hypercholesterolemia; Hyperemesis Gravidarum; Hyperexplexia; Hyperhidrosis, Primary; Hyperkalemia; Hyperlipoproteinemia Type III; Hyperlipoproteinemia Type IV; Hyperostosis Frontalis Interna; Hyperoxaluria, Primary (Type I); Hyperprolinemia Type I; Hyperprolinemia Type II; Hyperthermia; Hypochondroplasia; Hypoglycemia; Hypohidrotic Ectodermal Dysplasia; Hypokalemia; Hypomelanosis of Ito; Hypoparathyroidism; Hypophosphatasia; Hypophosphatemia, Familial; Hypoplastic Left Heart Syndrome; Hypotension, Orthostatic; Hypothyroidism; Hypotonia, Benign Congenital; I Cell Disease; IRF6-Related Disorders; Ichthyosis; Ichthyosis Hystrix, Curth Macklin Type; Ichthyosis Vulgaris; Ichthyosis, CHILD Syndrome; Ichthyosis, Chanarin Dorfman Syndrome; Ichthyosis, Erythrokeratodermia Progressiva Symmetrica; Ichthyosis, Erythrokeratodermia Variabilis; Ichthyosis, Erythrokeratolysis Hiemalis; Ichthyosis, Harlequin Type; Ichthyosis, Keratosis Follicularis Spinulosa Decalvans; Ichthyosis, Lamellar; Ichthyosis, Netherton Syndrome; Ichthyosis, Sjogren Larsson Syndrome; Ichthyosis, Trichothiodystrophy; Ichthyosis, X Linked; Idiopathic Pulmonary Fibrosis; IgA Nephropathy; Imperforate Anus; Incontinentia Pigmenti; Interstitial Cystitis; Intestinal Pseudoobstruction; Irritable Bowel Syndrome; Ivemark Syndrome; Jackson Weiss Syndrome; Jansen Type Metaphyseal Chondrodysplasia; Jarcho Levin Syndrome; Jejunal Atresia; Jervell and Lange-Nielsen Syndrome; Job Syndrome; Johanson Blizzard Syndrome; Joubert Syndrome; Jumping Frenchmen of Maine; KBG Syndrome; Kabuki Make-up Syndrome; Kallmann Syndrome; Kartagener Syndrome; Kawasaki Disease; Kearns Sayre Syndrome; Kennedy Disease; Kenny Caffey Syndrome; Keratitis Ichthyosis Deafness Syndrome; Keratoconjunctivitis, Vernal; Keratoconus; Keratomalacia; Keratosis Follicularis; Keratosis, Seborrheic; Kernicterus; Kienbock Disease; Kikuchi's Disease; Kleine Levin Syndrome; Klinefelter Syndrome; Klippel Trenaunay Syndrome; Klippel-Feil Syndrome; Kluver Bucy Syndrome; Kniest Dysplasia; Kohler Disease; Kufs Disease; Kugelberg Welander Syndrome; L1 Syndrome; LADD Syndrome; LEOPARD Syndrome; Laband Syndrome; Lactose Intolerance; Lambert-Eaton Myasthenic Syndrome; Landau Kleffner Syndrome; Langerhans Cell Histiocytosis; Laron Syndrome; Larsen Syndrome; Laurence Moon Syndrome; Leber Hereditary Optic Neuropathy; Leber's Congenital Amaurosis; Legg Calve Perthes Disease; Legionnaires' Disease; Leigh's Disease; Lennox Gastaut Syndrome; Lenz Microphthalmia Syndrome; Leprechaunism; Leprosy; Leptospirosis; Leri Pleonosteosis; Lesch Nyhan Syndrome; Leukemia, Chronic Lymphocytic; Leukemia, Chronic Myelogenous; Leukemia, Hairy Cell; Leukodystrophy; Leukodystrophy, Krabbe's; Leukodystrophy, Metachromatic; Lichen Planus; Lichen Sclerosus; Lipodystrophy; Lissencephaly; Listeriosis; Locked In Syndrome; Loken Senior Syndrome; Lowe Syndrome; Lupus; Lyme Disease; Lymphadenopathy, Angioimmunoblastic with Dysproteinemia; Lymphangioleiomyomatosis; Lymphatic Malformations; Lymphedema, Hereditary; Lymphocytic Infiltrate of Jessner; Lymphoma, Gastric, Non Hodgkins Type; Lynch Syndromes; Lysosomal Storage Disorders; MELAS Syndrome; MERRF Syndrome; MURCS Association; Machado-Joseph Disease; Macroglossia; Macular Degeneration; Madelung's Disease; Maffucci Syndrome; Mal de Debarquement; Malaria; Malignant Hyperthermia; Mallory Weiss Syndrome; Manic Depression, Bipolar; Mantle Cell Lymphoma; Maple Syrup Urine Disease; Marcus Gunn Phenomenon; Marden Walker Syndrome; Marfan Syndrome; Marinesco Sjogren Syndrome; Maroteaux Lamy Syndrome; Marshall Smith Syndrome; Marshall Syndrome; Mastocytosis; Maxillofacial Dysostosis; Maxillonasal Dysplasia, Binder Type; May Hegglin Anomaly; McCune Albright Syndrome; McKusick Type Metaphyseal Chondrodysplasia; Measles; Meckel Syndrome; Mediterranean Fever, Familial; Medium Chain Acyl CoA Dehydrogenase Deficiency; Medullary Cystic Kidney Disease/Nephronophthisis; Medullary Sponge Kidney; Medulloblastoma; Megalocornea Mental Retardation Syndrome; Meige Syndrome; Melanoma, Malignant; Meleda Disease; Melkersson Rosenthal Syndrome; Melnick Needles Syndrome; Membranoproliferative Glomerulonephritis Type II; Meniere Disease; Meningioma; Meningitis; Meningitis, Bacterial; Meningitis, Meningococcal; Meningitis, Tuberculous; Meningococcemia; Menkes Disease; Mesenteritis, Retractile; Mesothelioma; Metaphyseal Chondrodysplasia, Schmid Type; Metatropic Dysplasia I; Microvillus Inclusion Disease; Mikulicz Syndrome; Miller Syndrome; Mitral Valve Prolapse Syndrome; Mixed Connective Tissue Disease (MCTD); Moebius Syndrome; Monilethrix; Morquio Syndrome; Motor Neuron Disease; Mountain Sickness, Acute; Mowat-Wilson Syndrome; Moyamoya Syndrome; Mucha Habermann Disease; Mucolipidosis IV; Mucopolysaccharidoses; Mucopolysaccharidosis Type I; Mucopolysaccharidosis Type III; Mucous Membrane Pemphigoid; Mulibrey Nanism Syndrome (Perheentupa Syndrome); Mullerian Aplasia; Multiple Epiphyseal Dysplasia; Multiple Sclerosis; Multiple Sulfatase Deficiency; Multiple System Atrophy; Mulvihill Smith Syndrome; Mumps; Muscular Dystrophy, Becker; Muscular Dystrophy, Duchenne; Muscular Dystrophy, Emery Dreifuss; Muscular Dystrophy, Limb Girdle; Muscular Dystrophy, Oculo Gastrointestinal; Mutism, Selective; Myasthenia Gravis; Mycosis Fungoides; Myelodysplastic Syndromes; Myelofibrosis, Idiopathic; Myeloma, Multiple; Myhre Syndrome; Myoclonus, General; Myopathy, Congenital, Batten Turner Type; Myopathy, Desmin Storage; Myopathy, Scapuloperoneal; Myositis, Inclusion Body; Myotonia Congenita; Myotubular Myopathy; N-Acetyl Glutamate Synthetase Deficiency; Nager Syndrome; Nail Patella Syndrome; Narcolepsy; Nelson Syndrome; Nemaline Myopathy; Neonatal Lupus; Neu Laxova Syndrome; Neurasthenia; Neuroacanthocytosis; Neurodegeneration with Brain Iron Accumulation Type 1; Neurofibromatosis Type 1 (NF-1); Neurofibromatosis Type 2 (NF-2); Neuroleptic Malignant Syndrome; Neuromyotonia; Neuropathy, Ataxia and Retinitis Pigmentosa; Neuropathy, Congenital Hypomyelination; Neuropathy, Giant Axonal; Neuropathy, Hereditary Sensory, Type I; Neuropathy, Hereditary Sensory, Type II; Neuropathy, Hereditary Sensory, Type IV; Neuropathy, Peripheral; Neutropenia, Cyclic; Neutropenia, Severe Chronic; Nevoid Basal Cell Carcinoma Syndrome; Nezelof's Syndrome; Niemann Pick Disease; Nocardiosis; Nonketotic Hyperglycinemia; Noonan Syndrome; Norrie Disease; Nystagmus, Benign Paroxysmal Positional;Obsessive Compulsive Disorder; Ochoa Syndrome; Ocular Motor Apraxia, Cogan Type; Oculo-Dento-Digital Dysplasia; Oculocerebral Syndrome with Hypopigmentation; Oculocerebrocutaneous Syndrome; Olivopontocerebellar Atrophy, Hereditary; Ollier Disease; Opitz G/BBB Syndrome; Opportunistic Infections; Opsoclonus-Myoclonus Syndrome; Oral Facial Digital Syndrome; Organic Personality Syndrome; Ornithine Transcarbamylase Deficiency; Orocraniodigital Syndrome; Osgood Schlatter Condition; Osteogenesis Imperfecta; Osteomyelitis; Osteonecrosis; Osteopetrosis; Otopalatodigital Syndrome Type I and II; PEPCK Deficiency, Mitochondrial; POEMS Syndrome; Pachydermoperiostosis; Pachyonychia Congenita; Paget's Disease; Paget's Disease of the Breast; Pallister Hall Syndrome; Pallister Killian Mosaic Syndrome; Pallister W Syndrome; Pancreatic Islet Cell Tumor; Panic Anxiety Syndrome; Panniculitis, Idiopathic Nodular; Papillitis; Papillon Lefevre Syndrome; Paracoccidioidomycosis; Paramyotonia Congenita; Paraplegia, Hereditary Spastic; Parkinson's Disease; Parry Romberg Syndrome; Pars Planitis; Parsonage Turner Syndrome; Patulous Eustachian Tube; Pediatric Cardiomyopathy; Peeling Skin Syndrome; Pelizaeus Merzbacher Brain Sclerosis; Pemphigus; Penta X Syndrome; Pentalogy of Cantrell; Perisylvian Syndrome, Congenital Bilateral; Perniosis; Pertussis; Peutz Jeghers Syndrome; Peyronie Disease; Pfeiffer Syndrome Type I; Phelan-McDermid Syndrome; Phenylketonuria; Pheochromocytoma; Phocomelia Syndrome; Phosphoglycerate Kinase Deficiency; Pica; Pick's Disease; Pierre Robin Sequence; Pineal Cysts, Symptomatic; Pinta; Pityriasis Rubra Pilaris; Pleuropulmonary Blastoma; Pneumonia, Eosinophilic; Pneumonia, Interstitial; Poland Syndrome; Polyarteritis Nodosa; Polychondritis; Polycystic Kidney Diseases; Polycystic Liver Disease; Polycystic Ovary Syndrome; Polycythemia Vera; Polyglucosan Body Disease, Adult; Polymorphous Low-Grade Adenocarcinoma; Polymyalgia Rheumatica; Polymyositis; Pompe Disease; Porphyria; Porphyria Cutanea Tarda; Porphyria, ALA-D; Porphyria, Acute Intermittent; Porphyria, Congenital Erythropoietic; Porphyria, Hereditary Coproporphyria; Porphyria, Variegate; Post Polio Syndrome; Posterior Uveitis; Prader Willi Syndrome; Precocious Puberty; Primary Lateral Sclerosis; Primary Orthostatic Tremor; Proctitis; Progeria, Hutchinson Gilford; Progressive Myoclonus Epilepsy; Progressive Osseous Heteroplasia (POH); Progressive Supranuclear Palsy; Prostatitis; Proteus Syndrome; Prune Belly Syndrome; Pseudo Hurler Polydystrophy; Pseudoachondroplastic Dysplasia; Pseudocholinesterase Deficiency; Pseudohypoparathyroidism; Pseudomyxoma Peritonei; Pseudotumor Cerebri; Pseudoxanthoma Elasticum (PXE); Psittacosis; Psoriasis; Pterygium Syndrome, Multiple; Pulmonary Alveolar Proteinosis; Pulmonary Hypertension, Primary; Pulmonary Hypertension, Secondary; Pure Red Cell Aplasia, Acquired; Purpura, Henoch-Schonlein; Purpura, Idiopathic Thrombocytopenic; Purpura, Thrombotic Thrombocytopenic; Pyknodysostosis; Pyoderma Gangrenosum; Pyridoxine-Dependent Seizures; Pyruvate Carboxylase Deficiency; Pyruvate Dehydrogenase Deficiency; Pyruvate Kinase Deficiency; Q Fever; Rabies; Rabson-Mendenhall Syndrome; Radiation Syndromes; Ramsay-Hunt Syndrome; Rapp Hodgkin Syndrome; Raynaud's Disease and Phenomenon; Recurrent Respiratory Papillomatosis; Reflex Sympathetic Dystrophy Syndrome; Refsum Disease; Reiter's Syndrome; Renal Agenesis, Bilateral; Renal Glycosuria; Respiratory Distress Syndrome, Infant; Restless Legs Syndrome; Retinitis Pigmentosa; Retinoblastoma; Retinopathy of Prematurity; Retinopathy, Arteriosclerotic; Retinopathy, Diabetic; Retinopathy, Hypertensive; Retinoschisis; Retroperitoneal Fibrosis; Rett Syndrome; Reye Syndrome; Rh Disease; Rheumatic Fever; Rickets, Vitamin D Deficiency; Rieger Syndrome; Roberts Syndrome; Robinow Syndrome; Rocky Mountain Spotted Fever; Romano Ward Syndrome; Rosai-Dorfman Disease; Rosenberg Chutorian Syndrome; Roseola Infantum; Rothmund Thomson Syndrome; Roussy Levy Syndrome; Rubella; Rubella, Congenital; Rubinstein Taybi Syndrome; Russell Silver Syndrome (RSS); Ruvalcaba Syndrome; SHORT Syndrome; Saethre Chotzen Syndrome; Sakati Syndrome; Sandhoff Disease; Santavuori Disease; Sarcoidosis; Schindler Disease; Schinzel Giedion Syndrome; Schinzel Syndrome; Schwartz Jampel Syndrome; Scleroderma; Scott Craniodigital Syndrome; Seckel Syndrome; Seitelberger Disease (Infantile Neuroaxonal Dystrophy); Sennetsu Fever; Septooptic Dysplasia; Setleis Syndrome; Severe Combined Immunodeficiency; Sheehan Syndrome; Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD); Shwachman Syndrome; Sialadenitis; Sialidosis; Sickle Cell Disease; Simian B Virus Infection; Simpson Dysmorphia Syndrome; Singleton Merten Syndrome; Sinonasal Undifferentiated Carcinoma; Sirenomelia Sequence; Sjogren Syndrome; Sly Syndrome; Smallpox; Smith Lemli Opitz Syndrome; Smith Magenis Syndrome; Sneddon Syndrome; Sotos Syndrome; Spasmodic Dysphonia; Spasmodic Torticollis; Spina Bifida; Spinal Muscular Atrophy; Split Hand/Split Foot Malformation; Spondyloepiphyseal Dysplasia Tarda; Spondyloepiphyseal Dysplasia, Congenital; Sprengel Deformity; Stenosis, Spinal; Stevens Johnson Syndrome; Stickler Syndrome; Stiff Person Syndrome; Streptococcus, Group B; Sturge Weber Syndrome; Stuve-Wiedemann Syndrome; Subacute Sclerosing Panencephalitis; Succinic Semialdehyde Dehydrogenase Deficiency; Sudden Infant Death Syndrome; Summitt Syndrome; Susac Syndrome; Sutton Disease II; Sweet Syndrome; Syphilis, Acquired; Syphilis, Congenital; Syringobulbia; Syringomyelia; TORCH Syndrome; Tangier Disease; Tardive Dyskinesia ; Tarsal Tunnel Syndrome; Tarui Disease; Tay Sachs Disease; Telecanthus with Associated Abnormalities; Temporomandibular Joint Dysfunction (TMJ); Tethered Spinal Cord Syndrome; Tetrahydrobiopterin Deficiency; Tetralogy of Fallot; Thalamic Syndrome (Dejerine Roussy); Thalassemia Major; Thalassemia Minor; Three M Syndrome; Thrombocythemia, Essential; Thrombocytopenia Absent Radius Syndrome; Thrombocytopenia, Essential; Tietze Syndrome; Timothy Syndrome; Tinnitus; Tolosa Hunt Syndrome; Tongue Carcinoma; Tongue, Fissured; Tongue, Geographic; Tongue, Hairy; Tooth and Nail Syndrome; Tourette Syndrome; Townes Brocks Syndrome; Toxic Epidermal Necrolysis; Toxic Shock Syndrome; Toxocariasis; Toxoplasmosis; Transverse Myelitis; Treacher Collins Syndrome; Tricho Dento Osseous Syndrome; Trichorhinophalangeal Syndrome Type I; Trichorhinophalangeal Syndrome Type III; Trichotillomania; Trigeminal Neuralgia (Tic Douloureux); Trimethylaminuria; Triplo X Syndrome; Triploid Syndrome; Trismus Pseudocamptodactyly Syndrome; Trisomy; Trisomy 13 Syndrome; Trisomy 18 Syndrome; Tropical Sprue; Truncus Arteriosus; Tuberculosis; Tuberous Sclerosis; Tularemia; Turcot Syndrome; Turner Syndrome; Twin Twin Transfusion Syndrome; Typhoid; Tyrosinemia, Hereditary; Urticaria Pigmentosa; Urticaria, Cholinergic; Urticaria, Cold; Urticaria, Papular; Urticaria, Physical; Usher Syndrome; VACTERL Association; VACTERL with Hydrocephalus; Valinemia; Varicella Zoster; Vascular Malformations of the Brain; Vasculitis; Vasculitis, Cutaneous Necrotizing; Velocardiofacial Syndrome; Ventricular Septal Defects; Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD); Vitamin B12 Deficiency; Vitiligo; Vogt Koyanagi Harada Syndrome; Von Gierke Disease; Von Hippel Lindau Disease; Von Willebrand Disease; Vulvovaginitis; WAGR Syndrome; Waardenburg Syndrome; Waldenstrom's Macroglobulinemia; Waldmann Disease; Walker Warburg Syndrome; Wandering Spleen; Weaver Syndrome; Wegener's Granulomatosis; Weil Syndrome; Weill Marchesani Syndrome; Weismann Netter Stuhl Syndrome; Werdnig Hoffman Disease; Werner Syndrome; Wernicke-Korsakoff Syndrome; West Nile Encephalitis; West Syndrome; Whipple Disease; Wieacker Syndrome; Wiedemann Rautenstrauch Syndrome; Wildervanck Syndrome; Williams Syndrome; Wilms' Tumor; Wilson's Disease; Winchester Syndrome; Wiskott Aldrich Syndrome; Wolf Hirschhorn Syndrome; Wolff Parkinson White Syndrome; Wolfram Syndrome; Wyburn Mason Syndrome; X linked Juvenile Retinoschisis; X linked Lymphoproliferative Syndrome; XYY Syndrome; Xeroderma Pigmentosum; Yaws; Yellow Fever; Yellow Nail Syndrome; Yunis Varon Syndrome; Zellweger Syndrome; Zollinger Ellison Syndrome; sanitary preparations for medical use; chemical preparations for use in medicine; dietetic foods adapted for medical use; disinfectants for medical use; preparations for destroying vermin; fungicides for medical use; herbicides; diagnostic preparations for clinical or medical use; diagnostic preparations for veterinary use; pharmaceutical preparations, namely contrast agents for radiography, x-ray radiography, computer tomography, magnetic resonance imaging, magnetic resonance tomography; medical preparations for treatment or prevention of diseases of the mouth; and medical preparations for treatment or prevention of diseases of the skin |
