11801 to 11900 most common queries

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

• Ring Chromosome 1
• Chromosome 6 Ring Syndrome
• Chromosome 8-Derived Supernumerary Ring or Marker
• Familial or Sporadic Hemiplegic Migraine
• Radiation-Induced Meningioma
• Duane Retraction Syndrome Type 2
• 3p Deletion Syndrome
• Rare Hyperparathyroidism
• Commissural Lip Fistula
• Growth Delay due to Insulin-Like Growth Factor I Resistance
• PIBIDS Syndrome
• Rare Hyperthyroidism
• Congenital Cornea Plana
• Acquired Hemolytic Anemia
• Drug-Induced Autoimmune Hemolytic Anemia
• Uveal Coloboma - Cleft Lip and Palate - Intellectual Disability
• Benign Familial Neonatal Epilepsy
• Glial Tumor
• Anaplastic Oligodendroglioma
• Acquired Idiopathic Sideroblastic Anemia
• Cherubism
• Idiopathic Acute Eosinophilic Pneumonia
• Tumor of Endocrine Glands
• Extragonadal Germinoma
• Congenital Bilateral Absence of Vas Deferens
• Familial Abdominal Aortic Aneurysm
• Inherited Ichthyosis
• Familial Prostate Cancer
• Familial Medullary Thyroid Carcinoma
• Bilateral Massive Adrenal Hemorrhage
• Autosomal Dominant Progressive Nephropathy with Hypertension
• Caudal Regression Sequence
• Transient Familial Neonatal Hyperbilirubinemia
• Neutrophil Immunodeficiency Syndrome
• Hyper-IgM Syndrome with Susceptibility to Opportunistic Infections
• Genetic Anomaly of Leukocytes
• Arnold-Chiari Malformation Type 2
• Atrial Septal Defect Type Ostium Primum
• Chronic Chagas Disease with Heart Involvement
• Acute Chagas Disease without Heart Involvement
• Acute Chagas Disease with Heart Involvement
• Early Infantile Epileptic Encephalopathy with Suppression-Burst
• Pyridoxine-Dependent Epilepsy
• Atypical Hemolytic-Uremic Syndrome with Thrombomodulin Anomaly
• Atypical Hemolytic-Uremic Syndrome with C3 Anomaly
• Atypical Hemolytic-Uremic Syndrome with MCP or CD46 Anomaly
• Atypical Hemolytic-Uremic Syndrome with Anti-Factor H Antibodies
• Progressive Tubulointerstitial Nephropathy with Cholestatic Liver Disease
• Ledderhose Disease
• Atypical Glycine Encephalopathy
• Congenital Isolated ACTH Deficiency
• Adenohypophysitis
• Congenital Atransferrinemia
• Diffuse Alveolar Hemorrhage
• Calcified Aponeurotic Fibroma
• Hereditary Hypercarotenemia and Vitamin A Deficiency
• Familial Alzheimer-Like Prion Disease
• Legionellosis
• Maternally-Inherited Diabetes and Deafness
• Congenital Mesoblastic Nephroma
• Acute Endophthalmitis
• Extramammary Paget Disease
• Congenital Herpes Virus Infection
• Paroxysmal Dyskinesia
• Autosomal Recessive Stickler Syndrome Type 1
• Autosomal Dominant Rhegmatogenous Retinal Detachment
• Echinococcus Multilocularis Infection of Liver
• Interatrial Communication
• Congenital Tricuspid Stenosis
• Autosomal Dominant Severe Congenital Neutropenia
• Brucella Suis
• Larynx Atresia
• Congenital Laryngeal Cyst
• Atresia of Small Intestine
• Blindness - Scoliosis - Arachnodactyly Syndrome
• Invasive Non-Typhoidal Salmonellosis
• Typhoid Fever
• Central Polydactyly of Toes
• Autosomal Recessive Primary Microcephaly
• Spondyloepimetaphyseal Dysplasia Type Aggrecan
• Autosomal Dominant Distal Renal Tubular Acidosis
• Periventricular Leukomalacia
• Xanthinuria Type 2
• White Sponge Nevus
• Male Infertility due to Globozoospermia
• Familial Primary Pulmonary Hypoplasia
• Bronchiolitis obliterans with Obstructive Pulmonary Disease
• Autosomal Dominant Keratitis
• B-Cell Non-Hodgkin Lymphoma
• Alternating Hemiplegia of Childhood
• Retinitis pigmentosa 44
• Retinitis Pigmentosa 30
• Retinitis pigmentosa, Y-Linked
• Transient Congenital Hypothyroidism
• Long QT Syndrome 12
• Jervell and Lange-Nielsen Syndrome 2
• Long QT Syndrome 9
• Long QT Syndrome 8
• Pelizaeus-Merzbacher-like Brain Sclerosis
• Usher Syndrome Type 1H