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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