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Gangrene and Necrosis of the Lung Common Variable Immunodeficiency Chromosome 17p13.1 Deletion Syndrome Endometrial Carcinoma 46,XY Sex Reversal Type 6 FADD-Related Immunodeficiency Euphorbia Poisoning Autosomal Recessive Spastic Paraplegia Type 51 Reye Syndrome 1p32-p31 Deletion Syndrome Liver Failure Retinitis Pigmentosa Type 4 Adult-Onset Autosomal Recessive Cerebellar Ataxia Limb-Girdle Muscular Dystrophy Type 2Q Hepatocellular Carcinoma Early Infantile Epileptic Encephalopathy Type 12 Congenital Acquired Immune Deficiency Syndrome Aflatoxicosis Early Infantile Epileptic Encephalopathy Type 11 Foville Syndrome Factor I Deficiency Early Infantile Epileptic Encephalopathy Type 7 Urolithiasis Treacher-Collins Syndrome Type 2 Ligament Sprain Vitamin B12 Deficiency Hereditary Sensory and Autonomic Neuropathy Type 1D Afferent Loop Syndrome Aerophagy Long QT Syndrome 6 Long QT Syndrome 2 Typhus Spondylocostal Dysostosis Type 4 Facet Joint Syndrome Rheumatoid Arthritis 2q31.1 Duplication Syndrome Beta Blocker Poisoning Familial Hyperaldosteronism Type 3 Hypochondroplasia Familial Vesicoureteral Reflux Type 3 Dermatographia Congenital Dyserythropoietic Anemia Type 4 CINCA Syndrome Oligoarthritis Adult-Onset Still Disease Adult Neuronal Ceroid Lipofuscinosis Mitochondrial DNA Depletion Syndrome Type 4B Dementia Congenital Disorder of Glycosylation Type 1P Cone Rod Dystrophy Type 15 Adult Attention Deficit Disorder Brain Calcification Type Rajab Amaurotic Familial Idiocy Immunodeficiency due to a Classical Component Pathway Deficiency Autosomal Recessive Spastic Paraplegia Type 48 Primary Immune Deficiency Disorder Acquired Adrenogenital Syndrome Recessive Intermediate Charcot-Marie-Tooth Disease Type B Vocal Cord Nodule Primary Amenorrhea Hereditary Sensory and Autonomic Neuropathy Type 1C Multifocal Motor Neuropathy Precocious Puberty in Males Ambiguous Genitalia Agenesis of the Corpus Callosum and Congenital Lymphedema Congenital facial nerve palsy Autoimmune Encephalopathy Choanal Atresia and Lymphedema Cranioectodermal Dysplasia 2 Neurosarcoidosis Polycythemia Neonatorum Dermatofibrosarcoma Protuberans Adrenogenital Syndrome Nelson Syndrome Chromosome 4q32.1-q32.2 Triplication Syndrome Bilateral Adrenalectomy Occult Macular Dystrophy Adrenal Gland Neoplasm Retinitis Pigmentosa 57 Hypokalemic Periodic Paralysis Retinitis Pigmentosa 56 Steroid Withdrawal Syndrome Ectodermal Dysplasia - Cutaneous Syndactyly Syndrome Myopathy with Lactic Acidosis and Sideroblastic Anemia Type 2 Toxic Liver Disease Tuberculosis of Nervous System Adrenal Insufficiency Secondary to Hypopituitarism Senior-Boichis Syndrome Thyroid Dysfunction Retroperitoneal Hemorrhage Chromosome 6q11-q14 Deletion Syndrome Limb-Girdle Muscular Dystrophy Type 1H Autosomal Recessive Agammaglobulinemia Type 4 Autosomal Recessive Agammaglobulinemia Type 3 Malignant Neoplasm of Pancreas Common Variable Immunodeficiency Type 6 Common Variable Immunodeficiency Type 5 Common Variable Immunodeficiency Type 4 Common Variable Immunodeficiency Type 3 Chronic Eosinophilic Leukemia