Sitemap | Symptoma

17201 to 17300 most common queries

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

Pyloric Stenosis Gastroduodenal Perforation Congenital Lethal Myopathy Type Compton-North Mallory-Weiss Syndrome Inflammatory Bowel Disease Type 25 Leukemoid Reaction Ovarian Metastasis Autosomal Dominant Mental Retardation Type 5 Drayer Syndrome Gastric Ulcer 22q11.2 Duplication Syndrome Gastric Adenoma 15q11-q13 Duplication Syndrome Autosomal Recessive Deafness 1B Leber Congenital Amaurosis Type 13 Retrobulbar Neuritis Large Bowel Obstruction Kahrizi Syndrome Exfoliative Dermatitis Pancreatic Insufficiency - Anemia - Hyperostosis Syndrome Hydronephrosis Myopia Type 15 Direct Inguinal Hernia Autosomal Dominant Polycystic Kidney Disease Müllerian Aplasia - Hyperandrogenism Spinal Fractures Microdeletion 3q29 Syndrome Cutaneous T-Cell Lymphoma Adenocarcinoma of the Colon Faciocardiomelic Syndrome RAS-Associated Autoimmune Leukoproliferative Disease Multicentric Carpo-Tarsal Osteolysis with or without Nephropathy Loeys-Dietz Syndrome Type 2 Lower Gastrointestinal Hemorrhage Chylous Ascites Hereditary Spherocytosis Type 1 Chronic Immune Thrombocytopenic Purpura Inflammatory Bowel Disease Type 11 Perinephric Abscess Amelogenesis Imperfecta Type 1C Diffuse Large B-Cell Lymphoma Autosomal-Recessive Pyridoxine-Refractory Sideroblastic Anemia Diffuse Lymphoma Protein-Losing Enteropathy Bardet-Biedl Syndrome Type 14 Xanthomatosis Bardet-Biedl Syndrome Type 13 Cecal Disease Deafness, Autosomal Recessive, Type DFNB1A Dystonia with Cerebellar Atrophy (DYTCA) Spondylometaphyseal Dysplasia Type East African Cecal Adenocarcinoma Spondyloepiphyseal Dysplasia Type Cantú Staphylococcal Pneumonia Congenital Non-Goitrous Hypothyroidism Type 5 Phlegmasia Cerulea Dolens Horner's Syndrome Vulvitis Adrenal Gland Metastasis Atypical Krabbe Disease due to Saposin A Deficiency Volkmann's Contracture Progressive Myoclonic Epilepsy Type 3 Bronchial Adenocarcinoma Familial Cold Autoinflammatory Syndrome Type 2 Venous Insufficiency Cutaneous Metastasis in Breast Cancer Cauda Equina Syndrome LPAC Syndrome Type 1 Distal Hereditary Motor Neuropathy Type 2B Occult Malignancy Carney Complex Type 1 Urinary Calculus Self-limited Epilepsy with Centrotemporal Spikes Urethral Neoplasm Uremia Stickler Syndrome Type 1 Central Diabetes Insipidus Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency X-Linked Mental Retardation Type 93 Angiomyolipoma Leukoencephalopathy - Metaphyseal Chondrodysplasia Syndrome Subependymal Giant Cell Astrocytoma X-Linked Syndromic Mental Retardation Type 14 Malignant Ascites X-Linked Selective Tooth Agenesis Type 1 Leukoerythroblastic Anemia Potocki Lupski Syndrome Temporal Lobe Tumor Subacute Transverse Myelitis Thoracic Spinal Cord Tumor Interstitial Lung Disease due to ABCA3 Deficiency Cervical Spinal Cord Tumor Autosomal Dominant Coronary Artery Disease Type 2 Caudal Spinal Cord Tumor Pitt-Hopkins Syndrome Superior Vena Cava Syndrome Congenital Disorder of Glycosylation Type 2F Polymyositis Autosomal Recessive Proximal Renal Tubular Acidosis Malignant Pericardial Effusion