Sitemap | Symptoma 10401 to 10500 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Glycogen Storage Disease due to Aldolase A Deficiency Dehydrated Hereditary Stomatocytosis Rabson Mendenhall Syndrome Sarcotubular Myopathy Charcot-Marie-Tooth Disease Type 1C Charcot-Marie-Tooth Disease Type 1B Charcot-Marie-Tooth Disease Type 1A Juvenile Myoclonic Epilepsy Idiopathic Generalized Epilepsy Vitamin D Hydroxylation Deficient Rickets Type 1A Tyrosinemia Type 3 Acetyl-CoA Carboxylase Deficiency Glutaric Acidemia, Type 1 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome Pyroglutamate Hydrolase Deficiency Oculocutaneous Albinism, Type 2 Atypical Phenylketonuria Gitelman Syndrome Deficiency of Glycerol Kinase Trypsinogen Deficiency Muckle-Wells Syndrome Adult Junctional Epidermolysis Bullosa Autosomal Recessive Cutis Laxa Type 2A De Barsy Moens Diercks Syndrome Autosomal Recessive Cutis Laxa Type 1A Ehlers-Danlos Syndrome Periodontitis Type 1 Ehlers-Danlos Syndrome Arthrochalasia Type Brittle Cornea Syndrome Type 1 Ehlers-Danlos Syndrome Kyphoscoliotic Type 1 Ehlers-Danlos Syndrome Type 4 Ehlers-Danlos Syndrome Hypermobility Type Ehlers-Danlos Syndrom Classic Type 2 Acute Hepatic Porphyria Aagenaes Syndrome Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency GM1 Gangliosidosis Generalized Gangliosidosis Type II Generalized Gangliosidosis Farber Disease Gaucher Disease Type 3 Niemann-Pick Disease Type B Neutral Lipid Storage Disease Neuraminidase 1 Deficiency Cytochrome B5 Reductase Deficiency Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency Xeroderma Pigmentosum Complementation Group F Xeroderma Pigmentosum Complementation Group B Adenylosuccinate Lyase Deficiency Purine-Nucleoside Phosphorylase Deficiency Xanthinuria Type 1 Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency Familial Juvenile Hyperuricemic Nephropathy Type 1 Neonatal Hemochromatosis Congenital Sodium Diarrhea Congenital Chloride Diarrhea Hereditary Koilonychia Netherton Syndrome Erythrokeratodermia Variabilis et Progressiva Lymphedema Distichiasis Syndrome Coffin-Siris Syndrome Keratitis-Ichthyosis-Deafness Syndrome Tricho-Dento-Osseous Syndrome Moynahan Syndrome Baller-Gerold Syndrome Frontometaphyseal Dysplasia Atelosteogenesis Achondrogenesis, Type 1A Adams-Oliver Syndrome Grebe Syndrome Popliteal Pterygium Syndrome Genee-Wiedemann Syndrome Coffin-Lowry Syndrome Nager Syndrome Muscular Dystrophy-Dystroglycanopathy Type A Marshall-Smith Syndrome Weaver Syndrome Ringed Hair Disease McCune-Albright Syndrome Isaac Syndrome Benign Familial Hematuria Pick Disease of The Brain Welander Distal Myopathy Malignant Atrophic Papulosis Opitz-Kaveggia Syndrome Craniofrontonasal Dysplasia Congenital Adrenal Gland Hypoplasia Hereditary Multiple Intestinal Atresia Childhood-Onset Hypophosphatasia Familial Amniotic Bands Benign Familial Infantile Epilepsy Fatal Familial Insomnia Larsen's Syndrome LEOPARD Syndrome Sotos Syndrome Johanson-Blizzard Syndrome Adrenoleukodystrophy Polycystic Liver Disease Tooth Ankylosis Mucopolysaccharidosis 4A Autoimmune Polyendocrine Syndrome Type 1
