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19001 to 19100 most common queries

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

BSCL2-Related Neurologic Disorders Syndromic Mental Retardation Male Infertility with Monogenic Teratozoospermia Refractive Error Familial Partial Epilepsy Limb Ischemia WFS1-Related Disorders Hereditary Coagulation Disorder Small-Intestine Neuroendocrine Tumor Parenchymatous Neurosyphilis Monogenic Diabetes Non-A-E Hepatitis Mitochondrial DNA Deletion Syndrome Pre-Malignant Neoplasm Altered Metabolism of Coumarin Childhood Carcinoma of Unknown Primary Site KCNT1-Related Epilepsy Thiourea Tasting Urate-Binding Globulin Decreased Commensal Bacterial Infectious Disease TP63-Related Disorders Ring Corneal Ulcer Malignant Buccal Mucosa Neoplasm Acute Poisoning by Drugs with Membrane-Stabilizing Effect Eye Movement Disorder Emilin-1-Related Connective Tissue Disorder Pediatric Aortic Valve Stenosis Trochleitis GRIN1-Related Neurodevelopmental Disorder Visual Pathway Disorder Autoimmune Disease of the Gastrointestinal Tract Intermediate Charcot-Marie-Tooth Disease Familial Juvenile Hyperuricemic Nephropathy APOE p.Leu167del-Related Lipid Disorders Tubulinopathy Hereditary Neuropathy SOX2-Related Eye Disorders PNPLA6-Related Disorders TGFBI-Related Corneal Dystrophy Autoimmune Autonomic Ganglionopathy Caveolinopathy Autosomal Recessive Complex Spastic Paraplegia due to Kennedy Pathway Dysfunction Ovarian Sarcoma Dentin Hypersensitivity Autoimmune Disease of the Urogenital Tract Root Resorption COL4A1-Related Disorders Autoimmune Disease of the Blood Complement Component 8 Deficiency Basal Ganglia Cerebrovascular Disease Genetic Hyperferritinemia without Iron Overload Intermittent Angle-Closure Glaucoma Acquired Night Blindness Nerve Compression Crater-Like Holes of the Optic Disc Lymphocytes Absent Progesterone Resistance Frontonasal Dysplasia in Klippel-Feil Syndrome Branchial Arch Defects Mitochondrial DNA Maintenance Defects ATP7A-Related Copper Transport Disorders Extracranial Arteriovenous Malformation Familial Atypical Hemolytic-Uremic Syndrome Autosomal Recessive Cerebellar Ataxia COL6-Related Myopathy Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses Lymphoepithelial-Like Carcinoma Microphthalmia-Anophthalmia-Coloboma Spectrum Bone Remodeling Disorder Benign Immune Organ Neoplasm Aneruptive Fever Pediatric Acute-Onset Neuropsychiatric Syndrome Malignant Neoplasm of the Spinal Meninges Arachindonic Acid Deficiency Secondary Non-Traumatic Avascular Necrosis Focal Myoclonic Seizures Neoplasm of the Central Nervous System Recessive Intermediate Charcot-Marie-Tooth Disease Maligant Sensory System Neoplasm Cardiac Malformations Extracellular Cholesterol Esterification Disorder Primary Bacterial Infectious Disease Cerebellopontine Angle Embryonal Tumor Non-Syndromic Mental Retardation RASA1-Related Disorders Immune Defect due to Inosine Phosphorylase Deficiency Congenital Disorder of Glycosylation with Developmental Anomaly Childhood Malignant Pancreatic Neoplasm Malignant Neoplasm of the Lip and Oral Cavity Autoimmune Disease of the Peripheral Nervous System Hemoglobin Zurich Hamartomatous Lip Myeloid and Lymphoid Neoplasms with Eosinophilia - Abnormalities of PDGFRA - PDGFRB - FGFR1- PCM1-JAK2 LH Resistance Recurrent Hepatitis C Virus-Induced Liver Disease after Liver Transplantation Ganglion and Cyst of Synovium - Tendon - Bursa Specific Language Impairment Pediatric Interstitial Lung Disease Knuckle Pads Parotid Disease