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16001 to 16100 most common queries

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

Neuroleptic Malignant Syndrome Craniosytosis Type 4 X-Linked Mental Retardation Type 99 Amoxapine Orofacial Dyskinesia X-Linked Deafness 6 X-Linked Mental Retardation Type 98 X-linked Parkinsonism-Spasticity Syndrome X-Linked Charcot-Marie-Tooth Disease Type 6 Congenital Disorder of Glycosylation Type 2M Paroxysmal Nocturnal Hemoglobinuria Type 1 Secondary Pulmonary Hypertension Deafness - Dystonia - Cerebral Hypomyelination Amniotic Fluid Embolism Focal Epilepsy - Speech Disorder - Mental Retardation High Myopia-Sensorineural Deafness Syndrome Amniotic Band Oligohydramnios Bardet-Biedl Syndrome Type 18 Spontaneous Rupture of Membranes Amnionitis Retinitis Pigmentosa 66 Fetal Disorder Renal-Hepatic-Pancreatic Dysplasia 1 Adhesion of Amnion to Fetus Mandibular Hypoplasia - Deafness - Progeroid Syndrome Memory Impairment Ammonium Tetrathiomolybdate Leber Congenital Amaurosis Type 17 Ammonium Chloride Chemical Conjunctivitis Autosomal Dominant Hypocalcemia Type 1 Autosomal Recessive Epidermolysis Bullosa Simplex Developmental Dysplasia of the Hip Type 2 Craniosynostosis Type 3 Inhalation of Noxious Gases Neuronal Ceroid Lipofuscinosis Type 13 Acute Respiratory Distress Syndrome Familial Candidiasis Type 8 Exposure to Ammonia Bardet-Biedl Syndrome Type 17 Amitriptyline Pulmonary Fibrosis Iodine-Induced Hypothyroidism Muscular Dystrophy-Dystroglycanopathy Type C14 Iodide Poisoning Autosomal Recessive Spastic Paraplegia Type 57 Torsades De Pointes Smith-McCort Dysplasia Type 2 Graves Disease Amiodarone Erythema Nodosum Meckel Syndrome Type 1 Labyrinthitis Charcot-Marie-Tooth Disease Type 4B3 Respiratory Muscle Paralysis Anaerobic Bacterial Infection Myasthenic Crisis Congenital Reticular Ichthyosiform Erythroderma Familial Osteochondritis dissecans Aminoglycoside Antibiotic Autosomal Recessive Non-Syndromic Hydrocephalus Aminoaciduria Osteosclerotic Metaphyseal Dysplasia Disorder of Amino Acid Metabolism Platelet-Type Bleeding Disorder 15 Autosomal Recessive Dyskeratosis Congenita Type 5 Hyporeninemic Hypoaldosteronism Dominant Intermediate Charcot-Marie-Tooth Disease Type F Aminopyrine Campsis Radicans Muscular Dystrophy-Dystroglycanopathy Type A11 Cone Rod Dystrophy Type 17 Leishmaniasis Mitochondrial Complex 3 Deficiency Nuclear Type 5 Mitochondrial Complex 3 Deficiency Nuclear Type 4 Mitochondrial Complex 3 Deficiency Nuclear Type 3 Mitochondrial Complex 3 Deficiency Nuclear Type 2 Perforated Nasal Septum Autosomal Dominant Progressive External Ophthalmoplegia Type 6 Steel Syndrome Progressive Retinal Dystrophy due to Retinol Transport Defect Facial Dysmorphism-Immunodeficiency-Livedo-Short Stature Syndrome Skin Ulcer Autosomal Recessive Primary Microcephaly Type 10 Skin Disease Autosomal Recessive Osteopetrosis Type 8 Mucocutaneous Leishmaniasis Progressive External Ophthalmoplegia - Myopathy - Emaciation Syndrome Spermatogenic Failure Type 11 Veratrum Viride Celastrus Scandens Ameloblastic Fibrosarcoma Brachydactyly Type A1C Amegakaryocytic Thrombocytopenia Microcephalic Primordial Dwarfism Type Alazami Chronic Constrictive Pericarditis Distal Arthrogryposis Type 5D Congenital Stationary Night Blindness Type 1F Hemiplegia