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19101 to 19200 most common queries

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

Carotid Artery Disease DEAF1-Related Disorders Bleomycine-Resistant Testicular Cancer Adult Lymphoma Carcinoma Showing Thymus-Like Elements LDL Cholesterol Mildly Increased Down Syndrome-Like Appearance Autoimmune Disease of the Eyes - Ears - Nose - Throat Autoimmune Disease of the Endocrine System Congenital Muscular Dystrophy-Dystroglycanopathy Sensory Neuropathy with Spastic Paraplegia Epithelial-Subepithelial Corneal Dystrophy Childhood Cerebral Neoplasm Cranial or Spinal Nerve Neoplasm Acquired Metabolic Disease Luminal Breast Carcinoma Nasal Cavity Disorder Autosomal Recessive Non-Syndromic Sensorineural Deafness Type DFNB Maxillary Double Lip Lower Extremity-Predominant Spinal Muscular Atrophy Type 2 Depressed Scar Hereditary Angioedema with C1Inh Deficiency Isolated Asymptomatic Increase of Creatine Phosphokinase Autosomal Recessive Split Hand-Split Foot Malformation Decreased Platelet Adenylate Cyclase Activity Childhood Malignant Parathyroid Neoplasm Metastatic Insulinoma X-Linked Monogenic Disease Commissural Lip Pits Low IgD Levels Incisors, Long Upper Central Sodium Channelopathy-Related Small Fiber Neuropathy X-Linked Deafness Bronchiectasis in Ciliary Dyskinesia SCN1A-Related Seizure Disorders Ectoparasitic Infestation Hypergonadotropic Ovarian Failure Inability to Smell Butyl Mercaptan ATP1A3-Related Neurologic Disorders Diarrhea-Positive Hemolytic Uremic Syndrome Hepatitis B Reinfection after Liver Transplantation Reductional Transverse Limb Defects GDAP1-Related Hereditary Motor and Sensory Neuropathy Congenital Hiatus Hernia MED12-Related Disorders Complication of Organ Transplantation Fetal Nicotine Spectrum Disorder Cerebral Cavernous Malformations Carcinoma in Situ Primary Malignant Bone Neoplasm GNAS Inactivation Disorder Fragile Site FRAXD Disseminated Intravascular Coagulation in the Newborn Non-Syndromic Disorder of Testicular Development WAS-Related Disorders GM2-Gangliosidosis Types B - B1 - Ab Susceptibility to Wilms Tumor ALS2-Related Disorders Numeric Sex Chromosome Variations Plasma Protein Disorder Dominant Cleft Palate Brachydactyly due to the Absence of Distal Phalanges Congenital Absence of the Vas Deferens in Cystic Fibrosis Congenital Abnormality of the Nervous System Midface Dysplasia Inborn Error of Steroid Metabolism SLC39A14 Deficiency PNPLA6-Related Spastic Paraplegia - Distal Muscle Wasting Increased Platelet-Membrane Fluidity Autoimmune Gastrointestinal Dysmotility Abnormal Visual Accommodation Impairment of Oral Perception Y-Linked Monogenic Disease Myofibrillar Lysis Inborn Error of Metal Metabolism Cardiac Hydatid Cysts with Intracavitary Expansion FREM1-Related Autosomal Recessive Disorders ANO5-Related Muscle Diseases SYNE1 Deficiency Abnormal Retinal Correspondence Erythema of Acral Regions Undefined Platelet Disorder Autoimmune Disease of the Skin and Connective Tissue Autoimmune Disease of the Cardiovascular System CLCN-Related Osteopetrosis Neurometabolic Disorder due to Serine Deficiency Associative Agnosia Parents Smoking Pulmonary Artery Disease SALL4-Related Disorders Retinal Dystrophies Primarily Involving Bruch's Membrane Cranial Nerve Neoplasm SETBP1-Related Disorder Vascular Neoplasm Reproductive System Disease Platelet-Signal-Processing Defect Splenic Tuberculosis Creatine Deficiency Syndromes Neonatal-Period Electroclinical Syndrome Chronic Lymphocytic Leukemia - Small Lymphocytic Lymphoma