16801 to 16900 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Congenital Disorder of Glycosylation Type 2J
• Neoplasm of Ampulla of Vater
• Long QT Syndrome 13
• Malignant Hepatic Neoplasm
• Neoplasm of Nasal Cavity
• Early Infantile Epileptic Encephalopathy Type 5
• Intercostal Neuralgia
• 14q11-q22 Microdeletion Syndrome
• Microscopic Polyangiitis
• Dilated Cardiomyopathy 1R
• Homozygous Familial Hypercholesterolemia
• 15q24 Deletion Syndrome
• Early Infantile Epileptic Encephalopathy Type 10
• Warsaw Breakage Syndrome
• Autosomal Recessive Deafness 84
• Fanconi Anemia Complementation Group O
• Acute Amebic Dysentery
• Fanconi Renotubular Syndrome Type 2
• Perforated Diverticulum
• Syndromic Multisystem Autoimmune Disease
• Brachydactyly Type E2
• Distal Hereditary Motor Neuropathy Type 2C
• Maturity-Onset Diabetes of the Young Type 11
• Maturity-Onset Diabetes of the Young Type 10
• Viral Upper Respiratory Tract Infection
• Acute Subglottic Laryngitis
• Mild Mononeuropathy of the Median Nerve
• Nephronophthisis-Like Nephropathy
• Branch Retinal Vein Occlusion
• Muscular Dystrophy-Dystroglycanopathy Type C2
• Migraine without Aura
• Muscular Dystrophy-Dystroglycanopathy Type C3
• Muscular Dystrophy-Dystroglycanopathy Type B2
• Muscular Dystrophy-Dystroglycanopathy Type B1
• Muscular Dystrophy-Dystroglycanopathy Type A6
• Muscular Dystrophy-Dystroglycanopathy Type A5
• Muscular Dystrophy-Dystroglycanopathy Type B3
• Muscular Dystrophy-Dystroglycanopathy Type A2
• Common Variable Immunodeficiency Type 2
• Congenital Disorder of Glycosylation Type 1Q
• Mantle Cell Lymphoma
• Bardet-Biedl Syndrome Type 15
• Pilocytic Astrocytoma
• Keratosis Obturans
• Autosomal Dominant Polycystic Kidney Disease 1
• Genetic Mosaic
• TK2-Related Myopathic Mitochondrial DNA Depletion Syndrome
• Passovoy Factor Defect
• Polyarticular Juvenile Idiopathic Arthritis
• Common Variable Immunodeficiency Type 1
• Benign Familial Neonatal Epilepsy Type 1
• Myelophthisis
• Limb-Girdle Muscular Dystrophy Type 1E
• Autosomal Recessive Deafness 76
• Philadelphia Chromosome Positive Chronic Myeloid Leukemia
• Dentinogenesis Imperfecta Type 1
• Recurrent Small-Cell Carcinoma of the Lung
• Meconium Ileus
• Opitz G/BBB Syndrome Type 1
• Metastatic Ovarian Carcinoma
• Autosomal Dominant Spastic Paraplegia Type 37
• Autosomal Dominant Spastic Paraplegia Type 36
• Bardet-Biedl Syndrome Type 4
• Bardet-Biedl Syndrome Type 2
• Bardet-Biedl Syndrome Type 1
• Spinocerebellar Ataxia Type 30
• Generalized Myotonia of Thomsen
• Limb-Girdle Muscular Dystrophy Type 2D
• Fusarium Infection
• Pseudohypoparathyroidism Type 1C
• Condyloma Latum
• Focal Non-Epidermolytic Palmoplantar Keratoderma
• Quinine Poisoning
• Lymph Node Disorder
• Hereditary Factor X Deficiency
• Amelogenesis Imperfecta Type 1G with Nephrocalcinosis
• Adrenal Infarction
• Isolated Sulfite Oxidase Deficiency
• Hypogonadotropic Hypogonadism
• Myotonic Dystrophy Type 2
• Zlotogora-Ogur Syndrome
• Neurofibromatosis-Noonan Syndrome
• Hereditary Prosopagnosia
• Growth Hormone Deficiency
• Infantile-Onset Ascending Hereditary Spastic Paralysis
• Immunodeficiency by Defective Expression of HLA Class 2
• Autosomal Dominant Spastic Paraplegia Type 3
• Autosomal Dominant Spastic Paraplegia Type 17
• Leber Congenital Amaurosis Type 1
• Infantile Onset Autophagic Vacuolar Myopathy
• Usher Syndrome Type 2C
• Nephropathic Cystinosis
• Athetoid Cerebral Palsy
• Crigler-Najjar Syndrome Type 2
• Intracranial Mass
• Clark-Baraitser Syndrome
• Ruptured Ectopic Pregnancy
• Ectopic Pregnancy with Intrauterine Pregnancy
• Epidermolysis bullosa simplex with Muscular Dystrophy
• Retroverted Uterus