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16201 to 16300 most common queries

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

Congenital Disorder of Glycosylation Type 2L Syndromic Microphthalmia 11 Neonatal Hepatitis Autosomal Recessive Congenital Ichthyosis Type 8 Lymphoproliferative Syndrome 1 Cystic Lung Disease Kallmann Syndrome Type 4 Alpha-1 Antitrypsin Deficiency Congenital Cataract Complex Cortical Dysplasia with other Brain Malformations Type 7 Primary Coenzyme Q10 Deficiency Type 1 Alpers Syndrome UV-Sensitive Syndrome 1 Polycystic Dysgenetic Disease of Parotid Salivary Glands Syphilitic Alopecia Choroideremia - Deafness - Obesity Syndrome Congenital Alopecia Beta-Propeller Protein-Associated Neurodegeneration X-Linked Central Congenital Hypothyroidism with Late-Onset Macroorchidism Alopecia Universalis Microphthalmia with Linear Skin Defects Syndrome X-Linked Syndromic Mental Retardation Type 32 Follicular Mucinosis Congenital Disorder of Glycosylation Type 1S Tinea Capitis Alopecia Areata Autoimmune Thrombocytopenia Postaxial Polydactyly Type A5 Kallmann Syndrome Type 3 Penicillin Allergy Allergic Conjunctivitis Primary Ciliary Dyskinesia 18 Common Variable Immunodeficiency Type 7 Autosomal Recessive Spastic Paraplegia Type 49 Nasal Polyp Hypersensitivity Pancytopenia Nephronophthisis Type 15 Pulmonary Alveolar Proteinosis Autosomal Recessive Isolated Ectopia Lentis 2 Alkylating Agent Mitochondrial Complex 3 Deficiency Hypogonadotropic Hypogonadism Type 13 Cervical Osteoarthritis Spondyloepiphyseal Dysplasia Tarda Coronary Atherosclerosis Short Stature - Optic Atrophy - Pelger-Huët Anomaly Syndrome Osteochondral Loose Body Psoriatic Arthritis Charcot-Marie-Tooth Disease Type 4F Ankylosing Spondylitis Hypogonadotropic Hypogonadism Type 14 Familial Cortical Myoclonus Autosomal Recessive Spastic Paraplegia Type 56 Autosomal Recessive Spastic Paraplegia Type 55 Shoulder Osteoarthritis Autosomal Recessive Spastic Paraplegia Type 54 Arthritis of Knee Autosomal Recessive Spastic Paraplegia Type 53 Osteoarthritis of the Hip Hereditary Essential Tremor Type 4 Usher Syndrome Type 1K Neuronal Ceroid Lipofuscinosis Type 11 Lumbar Spondylosis Nephronophthisis Type 14 Aicardi-Goutières Syndrome Type 6 Hereditary Sensory and Autonomic Neuropathy Type 6 Nephrotic Syndrome Type 2 Autosomal Recessive Spastic Paraplegia Type 35 Charcot-Marie-Tooth Disease Type 1E Jalili Syndrome Ochronosis with Alkaptonuria Congenital Stationary Night Blindness Type 1A Familial Hypertrophic Cardiomyopathy Type 1 BIDS Syndrome Pseudohypoparathyroidism Type 1A Congenital Non-Goitrous Hypothyroidism Type 1 Metabolic Alkalosis Digitalis Toxicity Aicardi-Goutières Syndrome Type 2 Toxic Effect of Corrosive Alkalis Fanconi Anemia Complementation Group P Alglucerase Primary Hemochromatosis Type 1 Alexander Disease Early Infantile Epileptic Encephalopathy Type 1 Esophagitis Medicamentosa Complement Factor I Deficiency Aldrin Poisoning FGFR2-Related Bent Bone Dysplasia Diuretic Toxicity Cerebellar Ataxia - Neuropathy - Vestibular Areflexia Syndrome Aldehyde Congenital Stationary Night Blindness Type 1E Autosomal Dominant Mental Retardation Type 13 Vitamin B Deficiency Labrune Syndrome Chylomicronemia Syndrome Early Infantile Epileptic Encephalopathy Type 13 Rib Fracture