Sitemap | Symptoma 20301 to 20400 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Calciphylaxis Pontocerebellar Hypoplasia Type 2 Congenital Symmetric Circumferential Skin Creases Autosomal Dominant Sideroblastic Anemia Congenital Onychauxis Generalized Pustular Psoriasis Congenital Malformation of the Knee Joint Cardio-Facio-Cutaneous Syndrome Desbuquois Dysplasia Cerebro-Oculo-Facio-Skeletal Syndrome Hereditary Corneal Dystrophy Peripheral Arteriovenous Malformation Brachyolmia Congenital Scoliosis due to Bony Malformation Charcot-Marie-Tooth Disease Type 2 Aicardi-Goutières Syndrome Balint Syndrome 46,XY Complete Gonadal Dysgenesis Classic Migraine Lujan-Fryns Syndrome Drug-Induced Autoimmune Hemolytic Anemia Atrial Standstill Toxic Secondary Sideroblastic Anemia Secondary Sideroblastic Anemia due to Disease 46,XX Complete Gonadal Dysgenesis Congenital Stationary Night Blindness Congenital Stationary Night Blindness Type 2A West Syndrome Typhoid Fever Bladder Exstrophy Hyperleucinemia Periventricular Leukomalacia Male Infertility due to Globozoospermia Sitosterolemia Congenital Hypothyroidism without Goiter Epidermolysis Bullosa Simplex Folliculotropic Mycosis Fungoides Other Inherited Spinal Muscular Atrophy Bicornuate Uterus Leptin Receptor Deficiency Infantile - Juvenile - Presenile Cataracts Disorders of Pyruvate Metabolism and Gluconeogenesis Congenital Non-Progressive Ataxia Candidiasis of Skin and Nails Pervasive Developmental Disorder Asperger Syndrome Isolated Familial Somatotropinoma Gigantism - Acromegaly Neuronal Ceroid Lipofuscinosis Female with more than three X Chromosomes Partial Trisomy 13 in Patau Syndrome Minor Partial Trisomy Cyclopia Alobar Holoprosencephaly Adult-Onset Nemaline Myopathy Congenital Malformation Syndromes Involving Early Overgrowth Cystic Kidney Disease Congenital Malformation of the Corpus callosum Congenital Malformation Syndromes Affecting Facial Appearance Waardenburg Syndrome Type 2 Hypohidrotic Ectodermal Dysplasia Color Blindness Non-Immune Hydrops Fetalis Congenital Malformation Syndromes Predominantly Involving Limbs Hereditary Retinal Dystrophy Congenital Anomaly of the Retina Disorder of Copper Metabolism Congenital Malformation Syndromes Predominantly Associated with Short Stature Fragile X Chromosome Amyotrophic Lateral Sclerosis with Polyglucosan Bodies Hereditary Disturbances in Tooth Structure Disorders of Amino-Acid Transport Defects in Glycoprotein Degradation Glomerulosclerosis Feeding Problem Acute Renal Injury Schistocytosis Compulsive Disorder Streptococcal Pharyngitis Renal Insufficiency Normocytic Anemia Keratoconjunctivitis Sicca Pulmonary Vascular Disorders Temporal Headache Granulocytes Decreased Neuroaxonal Dystrophy Myokymia Focal Seizure Dysphasia Bronchoalveolar Lavage Abnormal Sclerosing Cholangitis Anterior Uveitis Hyperactive Deep Tendon Reflexes Fussiness Disorganized Behavior Euthymic Mood Soft Tissue X-Ray Abnormal Foreign Body Sensation Scedosporium Chronic Periodontitis
