Sitemap | Symptoma 16901 to 17000 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Progressive Familial Intrahepatic Cholestasis 4 Chronic Cervicitis Bulbourethral Gland Abscess Hawkinsinuria Lower Urinary Tract Infection Split Hand-Split Foot Malformation Type 1 Acute Nephritis Congenital Disorder of Glycosylation Type 2A Congenital Disorder of Glycosylation Type 1K Congenital Disorder of Glycosylation Type 1J Congenital Disorder of Glycosylation Type 1C Benign Essential Blepharospasm Adrenal Gland Disease Autosomal Recessive Deafness 88 Adrenal Hemorrhage Adrenal Destruction Autosomal Recessive Spastic Paraplegia Type 46 Hypertrophy of the Adrenal Cortex Xeroderma Pigmentosum Complementation Group C Osteopenia and Osteoporosis Hereditary Sensory and Autonomic Neuropathy Type 2A Purpura Adrenal Cortex Disease Giacheti Syndrome Folate-Deficiency Anemia Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency Congenital Disorder of Glycosylation Type 1T Autosomal Recessive Spastic Paraplegia Type 50 Adolescence Autosomal Recessive Cutis Laxa Type 2B Retinitis Pigmentosa 42 Tics Spastic Quadriplegic Cerebral Palsy Type 1 Adjustment Reaction of Adolescence Myoadenylate Deaminase Deficiency Intestinal Adhesions Overeating Pudendal Hernia Epileptic Encephalopathy with Global Cerebral Demyelination Chronic Appendicitis Congenital Deafness Ileal Crohn Disease Cataract Autosomal Recessive Parkinson Disease 14 Congenital Spinal Cord Anomaly Froehlich's Syndrome Myofibrillar Myopathy Type 6 Uterine Hypoplasia Obesity Optic Atrophy Type 7 Autosomal Dominant Emery-Dreifuss Muscular Dystrophy Esophageal Duplication Cleft Uvula Mesenteric Lymphadenitis Generalized Epilepsy with Febrile Seizures Plus Type 7 Viral Gastroenteritis Santos Syndrome Chromosome 19q13.11 Deletion Syndrome Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency Upper Respiratory Infection Genetic Combined Pituitary Hormone Deficiencies Neurodegenerative Syndrome due to Cerebral Folate Transport Deficiency Iritis Platelet-Type Bleeding Disorder 12 Viral Pneumonia TTR Amyloidosis with Polyneuropathy Bronchiolitis Bronchiectasis with or without Elevated Sweat Chloride 3 Epidemic Keratoconjunctivitis Hemivertebra Acute Laryngitis Autosomal Dominant Progressive External Ophthalmoplegia Type 5 Congenital Metatarsus Varus Leukopenia Basilar Artery Thrombosis Basilar Artery Occlusion Familial Juvenile Hyperuricemic Nephropathy Type 2 Internal Hemorrhoids Cone Dystrophy Type 4 Ruptured Sinus of Valsalva Acute Infectious Lymphocytosis Hallux Rigidus Acute Myocarditis Hereditary Hypotrichosis with Recurrent Skin Vesicles Achilles Tendon Rupture Ischemic Ulcer TUBB1-Related Autosomal Dominant Macrothrombocytopenia Vagina Carcinoma Hereditary Sensory and Autonomic Neuropathy Type 2B Carcinoma of Ampulla of Vater Adenovirus Infection Prostatism Severe Combined Immunodeficiency Infantile Dystonia - Parkinsonism Adenosine Deaminase Deficiency Inflammatory Bowel Disease Type 28 Muscular Dystrophy-Dystroglycanopathy Type B4 Herniated Disc Angina Pectoris Ruptured Cerebral Aneurysm
