15101 to 15200 most common queries

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

• Perforated Diverticulum
• Brachydactyly Type E2
• Distal Hereditary Motor Neuropathy Type 2C
• Maturity-Onset Diabetes of the Young Type 11
• Maturity-Onset Diabetes of the Young Type 10
• Nephronophthisis-Like Nephropathy
• Branch Retinal Vein Occlusion
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2N
• Common Migraine
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2O
• Muscle-Eye-Brain Disease Type A2
• Pilocytic Astrocytoma
• Genetic Mosaic
• TK2-Related Myopathic Mitochondrial DNA Depletion Syndrome
• Passovoy Factor Defect
• Myelophthisis
• Autosomal Recessive Deafness 76
• Dentinogenesis Imperfecta Type 1
• Recurrent Small-Cell Carcinoma of the Lung
• Meconium Ileus
• Autosomal Dominant Spastic Paraplegia Type 37
• Autosomal Dominant Spastic Paraplegia Type 36
• Bardet-Biedl Syndrome 2
• Spinocerebellar Ataxia Type 30
• Lymph Node Disorder
• Hereditary Factor X Deficiency
• Amelogenesis Imperfecta Type 1G with Nephrocalcinosis
• Isolated Sulfite Oxidase Deficiency
• Myotonic Dystrophy Type 2
• Hereditary Prosopagnosia
• Infantile-Onset Ascending Hereditary Spastic Paralysis
• Immunodeficiency by Defective Expression of HLA Class 2
• Autosomal Dominant Spastic Paraplegia Type 17
• Infantile Onset Autophagic Vacuolar Myopathy
• Clark-Baraitser Syndrome
• Ectopic Pregnancy with Intrauterine Pregnancy
• Retroverted Uterus
• Progressive Familial Intrahepatic Cholestasis 4
• Chronic Cervicitis
• Split Hand-Split Foot Malformation Type 1
• Acute Nephritis
• Congenital Disorder of Glycosylation Type 1c
• Benign Essential Blepharospasm
• Adrenal Gland Disease
• Autosomal Recessive Deafness 88
• Adrenal Destruction
• Autosomal Recessive Spastic Paraplegia Type 46
• Xeroderma Pigmentosum Complementation Group C
• Osteopenia and Osteoporosis
• Hereditary Sensory and Autonomic Neuropathy Type 2A
• Giacheti Syndrome
• Glycogen Storage Disease due to Phosphoglucomutase Deficiency
• Severe Intellectual Disability and Progressive Spastic Paraplegia
• Intestinal Adhesions
• Epileptic Encephalopathy with Global Cerebral Demyelination
• Crohn's Disease of Ileum
• Cataract
• Congenital Spinal Cord Anomaly
• Autosomal Recessive Optic Atrophy Type 7
• Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
• Esophageal Duplication
• Cleft Uvula
• Generalized Epilepsy with Febrile Seizures Plus Type 7
• Chromosome 19q13.11 Deletion Syndrome
• Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency
• Genetic Combined Pituitary Hormone Deficiencies
• Bronchiectasis with or without Elevated Sweat Chloride 3
• Autosomal Dominant Progressive External Ophthalmoplegia Type 5
• Familial Juvenile Hyperuricemic Nephropathy Type 2
• Internal Hemorrhoids
• Hereditary Hypotrichosis with Recurrent Skin Vesicles
• Vagina Carcinoma
• Hereditary Sensory and Autonomic Neuropathy Type 2B
• Infantile Dystonia - Parkinsonism
• Adenosine Deaminase Deficiency
• Ruptured Cerebral Aneurysm
• Adenosine
• Polymicrogyria with Optic Nerve Hypoplasia
• Adenomyosis Uteri
• Primary Ciliary Dyskinesia 13
• Adenomatous Colon Polyp
• Congenital Muscular Dystrophy with Integrin Alpha-7 Deficiency
• Congenital Muscular Dystrophy due to LMNA Mutation
• Autosomal Recessive Spastic Paraplegia Type 44
• Amelogenesis imperfecta Type Hypomaturation
• Venous Insufficiency of Leg
• Hereditary Factor XIII Subunit B Deficiency
• Cirrhosis-Dystonia-Polycythemia-Hypermanganesemia Syndrome
• Psychogenic Impotence
• Cyesiophobia
• Leber Congenital Amaurosis Typ 14
• Autosomal Recessive Spastic Paraplegia Type 18
• Vaginal Adenocarcinoma
• Mitochondrial DNA Depletion Syndrome Type 8
• Avascular Necrosis
• Preterm Labor
• Autosomal Recessive Myopia 18
• Congenital Fibrosis of Extraocular Muscles Type 3A
• Thyroid Cancer
• Isolated Congenital Hypoglossia or Aglossia