15701 to 15800 most common queries

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

• Platelet-Type Bleeding Disorder 18
• 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