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