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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