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15801 to 15900 most common queries

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

Whipple Disease Autosomal Dominant Deafness 33 High Output Heart Failure Neurocirculatory Asthenia X-Linked Keratosis Follicularis Spinulosa Decalvans Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency Anemarrhena Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Type 10B Androgen Therapy Linear Nevus Sebaceus Syndrome Complex Cortical Dysplasia with Other Brain Malformations Type 5 Cutaneous Larva Migrans Ancylostoma Caninum Moyamoya Disease with Early-Onset Achalasia Poor Response to Eculizumab Early Infantile Epileptic Encephalopathy Type 19 Focal/Diffuse Non-Epidermolytic Palmoplantar Keratoderma Nemaline Myopathy Type 9 Retinitis pigmentosa 68 Premature Ovarian Failure Type 9 Premature Ovarian Failure Type 8 Optic Atrophy-Intellectual Disability Syndrome Upper Airway Obstruction Hyperphosphatasia with Mental Retardation Type 4 Pancytopenia - Developmental Delay Syndrome Angioedema Auriculocondylar Syndrome 3 Analgesic Abuse Analbuminemia Perianal Warts Acquired Immunodeficiency Syndrome Anal Intercourse PDE4D Haploinsufficiency Syndrome Joubert Syndrome Type 22 Rectal Stenosis Squamous Cell Carcinoma of the Anus Rectal Pain COASY Protein-Associated Neurodegeneration Anagrelide Macrocephaly-Developmental Delay Syndrome Joubert Syndrome Type 21 Drug-induced Thrombocytopenia Anaerobic Streptococcus Hereditary Sensory Neuropathy Type 1F Congenital Dyserythropoietic Anemia Type 1 Autosomal Dominant Deafness 56 Autosomal Recessive Spastic Paraplegia Type 72 Gas Gangrene Subcutaneous Emphysema Hepatocellular Adenoma Immunodeficiency Type 17 Hepatoblastoma Fanconi Renotubular Syndrome Type 3 Liver Neoplasm L-Ferritin Deficiency Satyriasis Congenital Disorder of Glycosylation Type 1W Polycythemia Verheij Syndrome Common Variable Immunodeficiency Type 10 Motor Neuron Disease Nephrotic Syndrome Type 9 Paraplegia Retinitis pigmentosa 67 Autoimmune Lymphoproliferative Syndrome Type 3 Autism Spectrum Disorder - Epilepsy - Arthrogryposis  Familial Episodic Pain Syndrome Type 3 Familial Episodic Pain Syndrome Type 2 Pseudobulbar Palsy Hereditary Sensory and Autonomic Neuropathy Type 7 Paraparesis Ehlers-Danlos Syndrome Musculocontractural Type 2 Early-Onset Parkinson Disease 20 Atypical Juvenile Parkinsonism Progressive Bulbar Palsy Idiopathic CD4 Lymphocytopenia Parkinson-Dementia Syndrome Autosomal Recessive Mental Retardation Type 38 Oppenheim Disease Autosomal Dominant Mental Retardation Type 21 Glycogen Storage Disease Type 4 Tongue Amyloidosis Charcot-Marie-Tooth Disease Type 2R Idiopathic Basal Ganglia Calcification Type 5 Primary Ciliary Dyskinesia 25 Early Infantile Epileptic Encephalopathy Type 18 Early Infantile Epileptic Encephalopathy Type 17 Polyarthritis Intracerebral Hematoma Hypersplenism Mononeuritis Multiplex Mitochondrial Complex 3 Deficiency Nuclear Type 6 Proximal Renal Tubular Acidosis Primary Ciliary Dyskinesia 23 Papillary Muscle Dysfunction Primary Ciliary Dyskinesia 22 Tenosynovitis Catecholaminergic Polymorphic Ventricular Tachycardia Type 5 Intestinal Hypomotility Anasarca