Sitemap | Symptoma 17101 to 17200 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. 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 Autosomal Dominant Spastic Paraplegia Type 42
