19001 to 19100 most common queries

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

• BSCL2-Related Neurologic Disorders
• Syndromic Mental Retardation
• Male Infertility with Monogenic Teratozoospermia
• Refractive Error
• Familial Partial Epilepsy
• Limb Ischemia
• WFS1-Related Disorders
• Hereditary Coagulation Disorder
• Small-Intestine Neuroendocrine Tumor
• Parenchymatous Neurosyphilis
• Monogenic Diabetes
• Non-A-E Hepatitis
• Mitochondrial DNA Deletion Syndrome
• Pre-Malignant Neoplasm
• Altered Metabolism of Coumarin
• Childhood Carcinoma of Unknown Primary Site
• KCNT1-Related Epilepsy
• Thiourea Tasting
• Urate-Binding Globulin Decreased
• Commensal Bacterial Infectious Disease
• TP63-Related Disorders
• Ring Corneal Ulcer
• Malignant Buccal Mucosa Neoplasm
• Acute Poisoning by Drugs with Membrane-Stabilizing Effect
• Eye Movement Disorder
• Emilin-1-Related Connective Tissue Disorder
• Pediatric Aortic Valve Stenosis
• Trochleitis
• GRIN1-Related Neurodevelopmental Disorder
• Visual Pathway Disorder
• Autoimmune Disease of the Gastrointestinal Tract
• Intermediate Charcot-Marie-Tooth Disease
• Familial Juvenile Hyperuricemic Nephropathy
• APOE p.Leu167del-Related Lipid Disorders
• Tubulinopathy
• Hereditary Neuropathy
• SOX2-Related Eye Disorders
• PNPLA6-Related Disorders
• TGFBI-Related Corneal Dystrophy
• Autoimmune Autonomic Ganglionopathy
• Caveolinopathy
• Autosomal Recessive Complex Spastic Paraplegia due to Kennedy Pathway Dysfunction
• Ovarian Sarcoma
• Dentin Hypersensitivity
• Autoimmune Disease of the Urogenital Tract
• Root Resorption
• COL4A1-Related Disorders
• Autoimmune Disease of the Blood
• Complement Component 8 Deficiency
• Basal Ganglia Cerebrovascular Disease
• Genetic Hyperferritinemia without Iron Overload
• Intermittent Angle-Closure Glaucoma
• Acquired Night Blindness
• Nerve Compression
• Crater-Like Holes of the Optic Disc
• Lymphocytes Absent
• Progesterone Resistance
• Frontonasal Dysplasia in Klippel-Feil Syndrome
• Branchial Arch Defects
• Mitochondrial DNA Maintenance Defects
• ATP7A-Related Copper Transport Disorders
• Extracranial Arteriovenous Malformation
• Familial Atypical Hemolytic-Uremic Syndrome
• Autosomal Recessive Cerebellar Ataxia
• COL6-Related Myopathy
• Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses
• Lymphoepithelial-Like Carcinoma
• Microphthalmia-Anophthalmia-Coloboma Spectrum
• Bone Remodeling Disorder
• Benign Immune Organ Neoplasm
• Aneruptive Fever
• Pediatric Acute-Onset Neuropsychiatric Syndrome
• Malignant Neoplasm of the Spinal Meninges
• Arachindonic Acid Deficiency
• Secondary Non-Traumatic Avascular Necrosis
• Focal Myoclonic Seizures
• Neoplasm of the Central Nervous System
• Recessive Intermediate Charcot-Marie-Tooth Disease
• Maligant Sensory System Neoplasm
• Cardiac Malformations
• Extracellular Cholesterol Esterification Disorder
• Primary Bacterial Infectious Disease
• Cerebellopontine Angle Embryonal Tumor
• Non-Syndromic Mental Retardation
• RASA1-Related Disorders
• Immune Defect due to Inosine Phosphorylase Deficiency
• Congenital Disorder of Glycosylation with Developmental Anomaly
• Childhood Malignant Pancreatic Neoplasm
• Malignant Neoplasm of the Lip and Oral Cavity
• Autoimmune Disease of the Peripheral Nervous System
• Hemoglobin Zurich
• Hamartomatous Lip
• Myeloid and Lymphoid Neoplasms with Eosinophilia - Abnormalities of PDGFRA - PDGFRB - FGFR1- PCM1-JAK2
• LH Resistance
• Recurrent Hepatitis C Virus-Induced Liver Disease after Liver Transplantation
• Ganglion and Cyst of Synovium - Tendon - Bursa
• Specific Language Impairment
• Pediatric Interstitial Lung Disease
• Knuckle Pads
• Parotid Disease