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

Amelogenesis Imperfecta Type 2A5 Berry Aneurysm Helsmoortel-van der Aa Syndrome Coarctation of the Aorta Primary Ciliary Dyskinesia 29 Early Infantile Epileptic Encephalopathy Type 24 Congenital Diarrhea Type 7 Cone Rod Dystrophy Type 19 Early Infantile Epileptic Encephalopathy Type 23 Pulsating Exophthalmos Pontocerebellar Hypoplasia Type 2E Cavernous Sinus Aneurysm Renal Infarction Cholesterol Embolism Leriche Syndrome Mitochondrial Complex 3 Deficiency Nuclear Type 8 Early Infantile Epileptic Encephalopathy Type 21 Primary Pigmented Nodular Adrenocortical Disease 4 Xia-Gibbs Syndrome Exsanguination Autosomal Dominant Mental Retardation Type 24 Abdominal Aortic Aneurysm Mitochondrial Complex 3 Deficiency Nuclear Type 7 Left Ventricular Aneurysm Autosomal Recessive Mental Retardation Type 43 Anaesthetic Induction Agent Immunodeficiency Type 23 Abdominal Obesity - Metabolic Syndrome Type 3 Anesthetic Pontocerebellar Hypoplasia Type 9 Pontocerebellar Hypoplasia Type 10 General Anesthesia Autosomal Recessive Mental Retardation Type 42 Polyhydramnios Retinitis Pigmentosa 69 Anencephaly Multiple Types of Congenital Heart Defects 4 Stillbirth Desbuquois Dysplasia Type 2 Anemone Pulsatilla Hemosiderosis Complex Cortical Dysplasia with Other Brain Malformations Type 6 Hemochromatosis Common Variable Immunodeficiency Type 11 Sideroblastic Anemia Cerebral Thrombosis Bilateral Temporo-Occipital Polymicrogyria Transient Ischemic Attack Autosomal Dominant Giant Axonal Neuropathy Type 2  Posthemorrhagic Anaemia of the Newborn Ataxia-Telangiectasia-Like Disorder Type 1 Megaloblastic Anemia Megaloblastic Anaemia in Pregnancy Congenital Hypoplastic Anemia Congenital Disorder of Glycosylation Type 1Y Acquired Spherocytosis Acquired Toxic Hemolytic Anemia Desbuquois Syndrome Type 1 Cold Agglutinin Disease Autosomal Recessive Ocular Coloboma Immunodeficiency Type 27A Congenital Hemolytic Anemia Congenital Aplastic Anemia Amelogenesis Imperfecta Type 1A Paroxysmal Nocturnal Hemoglobinuria Invasive Pulmonary Aspergillosis Bardet-Biedl Syndrome Type 5 Seckel Syndrome Type 8 Generalized Peeling Skin Syndrome Eosinophilic Fasciitis X-Linked Mental Retardation Type 101 Acute Radiation Sickness X-Linked Mental Retardation Type 100 Aleukemic Leukemia Bardet-Biedl Syndrome Type 19 Precursor-Cell Lymphoblastic Leukemia Acute Myelocytic Leukemia Bardet-Biedl Syndrome Type 16 Hairy Cell Leukemia Primary Myelofibrosis Oculocutaneous Albinism Type 5 Bacterial Infections Uremic Anemia Primary Open-Angle Glaucoma Type 1P Distal Hereditary Motor Neuropathy Type 2D Aicardi-Goutières Syndrome Type 7 Seckel Syndrome Type 4 Malnutrition and Anemia Myopia Type 17 Anemia of Infection Autosomal Recessive Spastic Paraplegia Type 45 Refractory Anemia Autosomal Dominant Spastic Paraplegia Type 41 Cataract 21, multiple Types Congenital Non-Bullous Ichthyosiform Erythroderma ARCI2 Charcot-Marie-Tooth Disease Type 2I Y-Linked Deafness 1 Anemia due to Glutathione Metabolism Disorder Gastric Antral Vascular Ectasia Gaucher Disease