Sitemap | Symptoma

17501 to 17600 most common queries

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

Spondyloepimetaphyseal Dysplasia Type Shohat Acute Pericoronitis Congenital Disorder of Glycosylation Type 1B Odontoma Central Sleep Apnea Nephritis Pulmonary Edema Familial Hemiplegic Migraine Type 3 Sinus Arrhythmia High Altitude Pulmonary Edema Cerebral Edema Brachyphalangy Polydactyly and Tibial Aplasia/Hypoplasia Alkalosis Northern Epilepsy Cor Pulmonale High Altitude Cerebral Edema Respiratory Alkalosis Brachydactyly Coloboma and Anterior Segment Dysgenesis Ingrown Nail Retinal Cone Dystrophy Type 3A Spondyloepimetaphyseal Dysplasia Type Geneviève Myeloid Metaplasia Acute Mountain Sickness Familial Normophosphatemic Tumoral Calcinosis Hypoalbuminemia Camptodactyly - Tall Stature - Scoliosis - Hearing Loss Familial Isolated Arrhythmogenic Right Ventricular Dysplasia Type 11 Primary Pigmented Nodular Adrenocortical Disease 1 Acute Inflammation Combined Oxidative Phosphorylation Deficiency Type 3 Acute Infectious Disease Holoprosencephaly Type 5 Acute Disease Central Nervous System Disorder Autosomal Recessive Deafness 42 Myelitis Autosomal Recessive Deafness 46 Acute Disseminated Encephalomyelitis Short Stature and Facio-Auriculo-Thoracic Malformations Singh-Williams-McAlister Syndrome Premature Atrial Contractions Distal Myopathy Type 3 Microphthalmia Syndromic 6 Hypoxia Neuronal Ceroid Lipofuscinosis Type 10 Autosomal Dominant Progressive External Ophthalmoplegia Type 4 Hypomyelinating Leukodystrophy Type 5 Primary Open-Angle Glaucoma Type 1M Tachyarrhythmia Mediastinitis H Syndrome Maxillary Neoplasm Acute Cor Pulmonale Cerebral Hemorrhage Premature Chromatid Separation Trait Acromesomelic Dysplasia Type Maroteaux Surgical Bleeding Complication Mandibular Neoplasm Drotrecogin Alfa Bleeding Diathesis Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 2 Huntington Disease-Like 1 Pelvic Inflammatory Disease Citrullinemia Type 2 Malignant Gastric Neoplasm Limb-Mammary Syndrome Sialadenitis Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 2 Actinomycosis Mycetoma Myocarditis Fungal Arthritis Autosomal Dominant Spastic Paraplegia Type 8 Bovine Actinomycosis Lymphedema Pericardial Effusion ACHOO Syndrome Bacterial Endocarditis Spinal Epidural Abscess ADULT Syndrome Biliary Cirrhosis Systemic Amyloidosis Alopecia Areata Type 1 Sacroilitis Amyotrophic Lateral Sclerosis Type 1 Frontotemporal Dementia with Motor Neuron Disease Type 1 Cooks Syndrome Familial Hypobetalipoproteinaemia Type 1 Mucopolysaccharidosis 1 Hyperplasia of the Leydig Cells Spastic Ataxia with Congenital Miosis Pleurisy Pulmonary Nocardiosis Primary Basilar Impression Nocardia Infection Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma Brachydactyly Type A1 Brachydactyly Type A6 Langer Nishino Yamaguchi Syndrome Childhood-Onset Idiopathic Basal Ganglia Calcification