17101 to 17200 most common queries

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

• Prostatic Disease
• Primary Ciliary Dyskinesia 7
• Membranoproliferative Glomerulonephritis
• Yakut Short-Stature Syndrome
• Christianson Syndrome
• Acute Prostatitis
• X-Linked Hypospadias 1
• X-Linked Scapuloperoneal Myopathy
• Bone Metastasis
• X-Linked Myopathy with Postural Muscle Atrophy
• X-Linked Syndromic Mental Retardation Type Wu
• X-Linked Spinocerebellar Ataxia Type 5
• Urinary Retention
• Cranio-Facio-Skeletal Syndrome
• X-Linked Reducing-Body Myopathy 1A
• Vocal Cord Paralysis
• Deafness - Cataract - Retinitis pigmentosa - Sperm Abnormalities
• X-Linked Syndromic Mental Retardation Type Najm
• X-Linked Spastic Paraplegia Type 34
• Parathyroid Carcinoma
• X-Linked Erythropoietic Protoporphyria
• Camptodactyly Syndrome Type Guadalajara III
• Catecholaminergic Polymorphic Ventricular Tachycardia Type 2
• Lymphatic Malformation Type 2
• Stevenson Carey Syndrome
• Biliary Tract Hemorrhage
• Hunter-MacDonald Syndrome
• Pulmonary Infarction
• Thrombocytopenia Type 4
• Primary Coenzyme Q10 Deficiency Type 4
• Autosomal Recessive Spastic Paraplegia Type 39
• Optic Papillitis
• Lumbar Spinal Stenosis
• Hypocalcemia
• Amyotrophic Lateral Sclerosis Type 10
• Urethral Syndrome
• Secondary Biliary Cirrhosis
• ANE Syndrome
• Gallbladder Perforation
• Hypophosphatemic Rickets and Hyperparathyroidism
• Abscess of Salivary Gland
• Retinitis Pigmentosa 41
• Hypertrophy of Nasal Turbinates
• Reactive Depression
• Otosclerosis 8
• Acute Laryngitis and/or Tracheitis
• Unilateral Deafness with Delayed Endolymphatic Hydrops
• Degenerative Brain Disorder
• Familial Hypertrophic Cardiomyopathy Type 11
• Pancreatic Insufficiency
• Pancreatic Adenocarcinoma
• Familial Hypertrophic Cardiomyopathy Type 12
• Epidermolysis Bullosa-Pyloric Atresia
• Early Infantile Epileptic Encephalopathy Type 4
• Cul De Sac Mass
• Retinitis Pigmentosa 29
• Diastasis Recti and Weakness of the Linea Alba
• Coats Plus Syndrome
• Familial Atrial Fibrillation 6
• Ascites
• Hypomyelinating Leukodystrophy Type 4
• Autoimmune Hemolytic Anemia
• Familial Atrial Fibrillation 7
• Autosomal Recessive Congenital Ichthyosis Type 6
• Joubert Syndrome Type 9 
• Ovarian Pregnancy
• Riedel Thyroiditis
• Ectopic Pregnancy
• Dominant Hypophosphatemia with Nephrolithiasis or Osteoporosis
• Ovarian Adenoma
• Female Genital Cancer
• Ovarian Cyst Torsion
• Primary CD59 Deficiency
• Galactocele
• Ovarian Cyst
• Talipes Calcaneovalgus
• Tubo-Ovarian Abscess
• Secondary Aldosteronism
• Autosomal Dominant Spastic Paraplegia Type 38
• Ehlers-Danlos Syndrome Spondylodysplastic Type 3
• Adenocarcinoma of the Ovary
• Pontocerebellar Hypoplasia Type 2B
• Pathological Fracture
• Connective Tissue Disorder due to Lysyl Hydroxylase-3 Deficiency
• Endometriosis
• Hypermobility Syndrome
• Hypomyelinating Leukodystrophy Type 6
• Tendon Rupture
• 4H Syndrome
• Skeletal Defects, Genital Hypoplasia, and Mental Retardation
• Adenocarcinoma of the Prostate
• Diamond-Blackfan Anemia Type 1
• Essential Tremor
• 2p15-p16.1 Deletion Syndrome
• Psychogenic Pruritus
• Amelogenesis Imperfecta Type 2A2
• Muscle Rupture
• Gastropathy
• Familial Adenomatous Polyposis
• Dyschromatosis Universalis Hereditaria 1