16901 to 17000 most common queries

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

• Retroverted Uterus
• Progressive Familial Intrahepatic Cholestasis 4
• Chronic Cervicitis
• Bulbourethral Gland Abscess
• Hawkinsinuria
• Lower Urinary Tract Infection
• Split Hand-Split Foot Malformation Type 1
• Acute Nephritis
• Congenital Disorder of Glycosylation Type 2A
• Congenital Disorder of Glycosylation Type 1K
• Congenital Disorder of Glycosylation Type 1J
• Congenital Disorder of Glycosylation Type 1C
• Benign Essential Blepharospasm
• Adrenal Gland Disease
• Autosomal Recessive Deafness 88
• Adrenal Hemorrhage
• Adrenal Destruction
• Autosomal Recessive Spastic Paraplegia Type 46
• Hypertrophy of the Adrenal Cortex
• Xeroderma Pigmentosum Complementation Group C
• Osteopenia and Osteoporosis
• Hereditary Sensory and Autonomic Neuropathy Type 2A
• Purpura
• Adrenal Cortex Disease
• Giacheti Syndrome
• Folate-Deficiency Anemia
• Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency
• Congenital Disorder of Glycosylation Type 1T
• Autosomal Recessive Spastic Paraplegia Type 50
• Adolescence
• Autosomal Recessive Cutis Laxa Type 2B
• Retinitis Pigmentosa 42
• Tics
• Spastic Quadriplegic Cerebral Palsy Type 1
• Adjustment Reaction of Adolescence
• Myoadenylate Deaminase Deficiency
• Intestinal Adhesions
• Overeating
• Pudendal Hernia
• Epileptic Encephalopathy with Global Cerebral Demyelination
• Chronic Appendicitis
• Congenital Deafness
• Ileal Crohn Disease
• Cataract
• Autosomal Recessive Parkinson Disease 14
• Congenital Spinal Cord Anomaly
• Froehlich's Syndrome
• Myofibrillar Myopathy Type 6
• Uterine Hypoplasia
• Obesity
• Optic Atrophy Type 7
• Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
• Esophageal Duplication
• Cleft Uvula
• Mesenteric Lymphadenitis
• Generalized Epilepsy with Febrile Seizures Plus Type 7
• Viral Gastroenteritis
• Santos Syndrome
• Chromosome 19q13.11 Deletion Syndrome
• Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency
• Upper Respiratory Infection
• Genetic Combined Pituitary Hormone Deficiencies
• Neurodegenerative Syndrome due to Cerebral Folate Transport Deficiency
• Iritis
• Platelet-Type Bleeding Disorder 12
• Viral Pneumonia
• TTR Amyloidosis with Polyneuropathy
• Bronchiolitis
• Bronchiectasis with or without Elevated Sweat Chloride 3
• Epidemic Keratoconjunctivitis
• Hemivertebra
• Acute Laryngitis
• Autosomal Dominant Progressive External Ophthalmoplegia Type 5
• Congenital Metatarsus Varus
• Leukopenia
• Basilar Artery Thrombosis
• Basilar Artery Occlusion
• Familial Juvenile Hyperuricemic Nephropathy Type 2
• Internal Hemorrhoids
• Cone Dystrophy Type 4
• Ruptured Sinus of Valsalva
• Acute Infectious Lymphocytosis
• Hallux Rigidus
• Acute Myocarditis
• Hereditary Hypotrichosis with Recurrent Skin Vesicles
• Achilles Tendon Rupture
• Ischemic Ulcer
• TUBB1-Related Autosomal Dominant Macrothrombocytopenia
• Vagina Carcinoma
• Hereditary Sensory and Autonomic Neuropathy Type 2B
• Carcinoma of Ampulla of Vater
• Adenovirus Infection
• Prostatism
• Severe Combined Immunodeficiency
• Infantile Dystonia - Parkinsonism
• Adenosine Deaminase Deficiency
• Inflammatory Bowel Disease Type 28
• Muscular Dystrophy-Dystroglycanopathy Type B4
• Herniated Disc
• Angina Pectoris