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17901 to 18000 most common queries

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Methylmalonic Aciduria Type cblA Conjunctivitis Rhinophyma Autosomal Recessive Primary Microcephaly Type 1 Microcephaly with Spastic Quadriplegia Keratitis Isolated Succinate-CoQ Reductase Deficiency Seborrheic Blepharitis Molybdenum Cofactor Deficiency Type B Molybdenum Cofactor Deficiency Type A Seborrheic Dermatitis Mucus Inspissation of Respiratory Tract Lethal Multiple Pterygium Syndrome Rosacea Lethal Congenital Contracture Syndrome 1 Chudley-Rozdilsky Syndrome Acne Necrotica Miliaris Wiedemann-Steiner Syndrome Autosomal Recessive Spastic Paraplegia Type 14 MYH9-Related Disorder Photosensitivity Disorder Spinocerebellar Ataxia Type 13 Diffuse Idiopathic Skeletal Hyperostosis Mesomelic Dysplasia Type Savarirayan Acitretin Autosomal Dominant Spastic Paraplegia Type 13 Hypervitaminosis A Chronic Rhinitis Tuberous Sclerosis Type 1 Respiratory Acidosis Charcot-Marie-Tooth Disease Type 4G Macrocephaly - Intellectual Disability - Autism Frontoocular Syndrome Electrolyte Imbalance Nemaline Myopathy Type 5 Spinocerebellar Ataxia Type 14 Hyperventilation Cone Rod Dystrophy Type 8 Charcot-Marie-Tooth Disease Type 2B1 Charcot-Marie-Tooth Disease Type 2B2 Dentinogenesis Imperfecta Type 1 with Autosomal Dominant Deafness 39 Organic Brain Syndrome Osteomalacia Late-Onset Retinal Degeneration Intracranial Hemorrhage Hyperkalemia Hypercapnia Distal Spinal Muscular Atrophy Type 2 Benign Familial Infantile Epilepsy Type 2 Congenital Onychodysplasia Congenital Slow-Channel Myasthenic Syndrome Type 4A Confusion Neonatal Onset Citrullinemia Type 2 Sinus Arrest Nonaka Myopathy Multifocal Atrial Tachycardia Metabolic Encephalopathy Intellectual Developmental Disorder with Autism and Speech Delay Congenital Disorder of Glycosylation Type 2B Charcot-Marie-Tooth Disease Type 2C Acidaminococcus Rippling Muscle Disease Type 2 Baraitser-Winter Syndrome 1 Tooth Erosion Sener Syndrome Acidifying Agent Poisoning Neuroferritinopathy Cholecystitis Dental Caries Acid Base Disorder Chromosome 22q13.3 Deletion Syndrome Generalized Motor Seizure Kondoh Syndrome Cholangitis Developmental Disabilities Seizure Cardiac Arrest Juvenile Primary Lateral Sclerosis Charcoal Premature Ventricular Contraction Cervicitis Generalized Epilepsy with Febrile Seizures-plus Type 4 Cerebrovascular Disorder Precalcaneal Congenital Fibrolipomatous Hamartoma Platelet-Type Bleeding Disorder 8 Central Retinal Artery Occlusion Acid-Base Imbalance Hereditary Hypophosphatemic Rickets with Hypercalciuria Lysosomal Acid Phosphatase Deficiency Autosomal Dominant Spastic Paraplegia Type 33 Spinocerebellar Ataxia Type 23 Acute Respiratory Failure Glycogen Storage Disease Type 2 Carotid Artery Thrombosis Autosomal Dominant Spastic Paraplegia Type 31 Autosomal Recessive Frontotemporal Pachygyria Asthenia Retinitis Pigmentosa 35 Cold-Induced Sweating Syndrome Type 2 Rhizomelic Dysplasia - Scoliosis - Retinitis Pigmentosa