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Craniosynostosis with Ocular Abnormalities and Hallucal Defects Jaundice Autosomal Dominant Coronary Artery Disease 1 Sudden Death Dominant Intermediate Charcot-Marie-Tooth Disease Type C Liver Abscess Recessive Intermediate Charcot-Marie-Tooth Disease Type A Peritoneal Disease Autosomal Dominant Congenital Nystagmus 3 Lesser Sac Abscess Hyaline Body Myopathy Spondyloepiphyseal Dysplasia Type Kimberley Rectovaginal Fistula Autosomal Recessive Primary Microcephaly Type 6 CD36 Deficiency Braddock Syndrome Ischiorectal Abscess Limb-Girdle Muscular Dystrophy Type 1F Mesenteric Vein Thrombosis Cystitis Juvenile Onset Primary Open-Angle Glaucoma Type 1 Familial Progressive Cardiac Conduction Defect Type 2 Intraperitoneal Abscess in the Right Lower Quadrant Familial Acne Inversa Familial Progressive Hyper- and Hypopigmentation Single Central Maxillary Incisor Coma Congenital Autosomal Dominant Indifference to Pain Ischio-Coxo-Podo-Patellar Syndrome Stupor Intracranial Abscess X-Linked Diffuse Leiomyomatosis-Alport Syndrome Low-Molecular-Weight Proteinuria with Hypercalciuria and Nephrocalcinosis 46,XY Sex Reversal Type 8 Biliary Colic X-Linked Syndromic Mental Retardation Type Wilson-Turner Prieto Syndrome Extrahepatic Cholestasis X-Linked Congenital Nystagmus Type 1 X-Linked Charcot-Marie-Tooth Disease Type 5 Properdin Deficiency Pericholecystic Abscess Early Infantile Epileptic Encephalopathy Type 2 X-Linked Spastic Paraplegia Type 2 Taurodontism Microdontia and Dens Invaginatus Widow's Peak Syndrome Tetanus Myopathy and Diabetes mellitus Lung Abscess Parapharyngeal Abscess Isolated Complex 1 Deficiency Lethal Infantile Mitochondrial Myopathy Atypical Facial Pain Hypocalcemic Vitamin D-Dependent Rickets Type 1B Maxillary Sinusitis Warburg Sjo Fledelius Syndrome Rhizomelic Chondrodysplasia Punctata Type 3 Periapical Abscess Retinitis Pigmentosa 11 CARASIL Pelvic Abscess Neuronal Ceroid Lipofuscinosis Type 7 Neuronal Ceroid Lipofuscinosis Type 8 Urticaria Rapidly Progressive Glomerulonephritis Distal Hereditary Motor Neuropathy Type 8 Shock Pachygyria-Mental Retardation-Seizures Uterine Fibroid Oculomaxillofacial Dysostosis Gastrocolic Fistula Toriello-Lacassie-Droste Syndrome Acute Pancreatitis Macrocephaly Type Fryns Multiple Epiphyseal Dysplasia Type 1 Intestinal Obstruction Enteropathy, Familial with Villous Edema and IgG2 Deficiency Spinal Muscular Atrophy Type 4 Arthritis Autosomal Dominant Spastic Paraplegia Type 6 Increased Sweating CODAS Syndrome Hereditary Hemorrhagic Telangiectasia Type 2 Gram-Negative Septicaemia Mesomelia-Synostoses Syndrome Abdominal Visceral Abscess Zori-Stalker-Williams Syndrome Myopathy with Lactic Acidosis and Sideroblastic Anemia Type 1 Autosomal Dominant Lateral Temporal Lobe Epilepsy Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 1 Autosomal Recessive Mental Retardation Type 3 Threatened Abortion Lattice Corneal Dystrophy Type 3A Congenital Corneal Opacities - Cornea Guttata - Corectopia Uterine Prolapse Polycythemia Type Chuvash Endometritis Leber Congenital Amaurosis Type 9 Familial Sick Sinus Syndrome Therapeutic Abortion