11301 to 11400 most common queries

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

• New-Onset Refractory Status Epilepticus
• Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome
• Familial Benign Flecked Retina
• Acute Infantile Liver Failure-Multisystemic Involvement Syndrome
• Mixed Functioning Pituitary Adenoma
• Congenital Thyroid Malformation without Hypothyroidism
• Venezuelan Hemorrhagic Fever
• Familial Papillary or Follicular Thyroid Carcinoma
• Translocation Renal Cell Carcinoma
• Hantavirus Pulmonary Syndrome
• Retinal Macular Dystrophy Type 2
• Constitutional Megaloblastic Anemia due to Folate Metabolism Disorder
• X-linked Cleft Palate and Ankyloglossia
• Chikungunya
• Hendra Virus Infection
• Leydig Cell Hypoplasia due to LHB Deficiency
• Immunoglobulin-Mediated Membranoproliferative Gomerulonephritis
• Acute Nephritic Syndrome with Diffuse Membranoproliferative Glomerulonephritis
• Lipoprotein Glomerulopathy
• Hemoglobin Lepore-Beta-Thalassemia Syndrome
• Immunodeficiency due to MASP-2 Deficiency
• Immunodeficiency Predominantly Affecting Antibody Production
• Efavirenz Toxicity
• Familial Congenital Mirror Movements
• Generalized Dominant Dystrophic Epidermolysis bullosa
• Congenital Trigeminal Anesthesia
• Atypical Teratoid Rhabdoid Tumor
• Familial Hypocalciuric Hypercalcemia Type 3
• Familial Cerebral Saccular Aneurysm
• Chronic Diarrhea with Villous Atrophy
• Alpha-Thalassemia - Myelodysplasia Syndrome
• Idiopathic Orthostatic Hypotension
• Benign Familial Infantile Epilepsy
• Leiomyoma of Vulva and Esophagus
• Non-Brugada-Type Idiopathic Ventricular Fibrillation
• Acquired Cutis Laxa
• Anetoderma Type Jadassohn-Pellizzari
• Anetoderma Type Schweninger-Buzzi
• Food-Borne Botulism
• Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
• Familial Pancreatic Carcinoma
• Isolated Klippel-Feil Syndrome
• Butyrylcholinesterase Deficiency
• Primary Fanconi Syndrome
• Primary Syringomyelia
• Anophthalmia - Microphthalmia Syndrome
• Congenital Cystic Eyeball
• Autosomal Dominant Larsen Syndrome
• Classic Hodgkin Lymphoma
• Neuroepithelioma
• Acute Lymphoblastic Leukemia with Lymphomatous Features
• Hereditary Breast Cancer
• Toxic Oil Syndrome
• Fowler Syndrome
• Familial Cerebral Cavernous Malformation
• Dural Sinus Malformation
• Anemia due to Adenosine Triphosphatase Deficiency
• Cranial Neuralgia
• Hyperdibasic Aminoaciduria Type 1
• Lysinuric Protein Intolerance
• Laron Syndrome with Immunodeficiency
• Dicarboxylic Aminoaciduria
• Hyperlysinemia Type 1
• Congenital Fibrinogen Deficiency
• Plague
• Aortopulmonary Fistula
• Familial Pulmonary Arterial Hypertension
• Double Outlet Left Ventricle
• Aortic Arch Interruption
• Combined Oxidative Phosphorylation Defect Type 8
• Discrete Fibromuscular Subaortic Stenosis
• Sensorineural Deafness with Dilated Cardiomyopathy
• Abnormal Number of Coronary Ostia
• Congenital Pulmonary Valve Insufficiency
• Pulmonary Atresia with Ventricular Septal Defect
• Abnormal Origin of the Pulmonary Artery
• Neonatal Acute Respiratory Distress due to SP-B Deficiency
• Pulmonary Interstitial Glycogenosis
• Microsporidiosis
• Hantavirosis
• Congenital Microcoria
• Cysticercosis of Eye
• West African Trypanosomiasis
• Glycogen Storage Disease due to GLUT2 Deficiency
• Acrofacial Dysostosis Type Palagonia
• Familial Glucocorticoid Deficiency
• Ring Chromosome 17
• Double Uterus - Hemivagina - Renal Agenesis Syndrome
• Aorto-Left Ventricular Tunnel
• Congenital Pulmonary Valve Stenosis
• Uterine Sarcoma
• Subpulmonary Stenosis
• Absence of Innominate Vein
• Congenital Pulmonary Veins Atresia or Stenosis
• Susceptibility to Malignant Cutaneous Melanoma 9
• Familial Atypical Multiple Mole Melanoma Syndrome
• Familial Melanoma
• Familial Melanoma of the Eyelid
• Familial Melanoma of the Lip
• Rhizomelic Chondrodysplasia Punctata