Sitemap | Symptoma 17301 to 17400 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Familial Progressive Cardiac Conduction Defect Choreoathetosis - Hypothyroidism - Neonatal Respiratory Distress Dermatomyositis Frontal Lobe Neoplasm Autosomal Recessive Deafness 24 Toxocariasis Syndrome of Inappropriate Antidiuretic Hormone Secretion Exposure to Toxin Hypercalcemia Tobacco Use Disorder Metastatic Skin Carcinoma Distal Spinal Muscular Atrophy Type 4 Tobacco Disseminated Intravascular Coagulation Autosomal Recessive Mental Retardation Type 5 Thyrotoxicosis Metastatic Liver Carcinoma Thyroiditis Breast Abscess Thrombophlebitis Thrombocytosis Retinitis Pigmentosa 37 Brachial Plexus Neuropathy Metastatic Adenocarcinoma of the Breast Breast Fibroadenoma Breast Hematoma Autosomal Dominant Spastic Ataxia Type 1 Fat Necrosis of the Breast Hamamy Syndrome Thalassemia Breast Hamartoma Charcot-Marie-Tooth Disease Type 4J Autosomal Recessive Spastic Paraplegia Type 32 Microglandular Adenosis Fibrocystic Breast Disease Focal Task Specific Dystonia Autosomal Recessive Spastic Ataxia Type 2 Carcinoma of the Male Breast Limb-Girdle Muscular Dystrophy Type 2L Splenic Metastasis Testicular Neoplasm Secondary Syphilis of Skin Cardiac Metastasis Mungan Syndrome Brachydactyly Type B2 Adenocarcinoma of the Breast Autosomal Recessive Spastic Ataxia with Leukoencephalopathy Legius Syndrome Autosomal Dominant Mental Retardation Type 1 Mitochondrial Trifunctional Protein Deficiency Gastric Dilatation Bladder Neck Obstruction Tyrosine Kinase 2 Deficiency Staphylococcal Infection Pontocerebellar Hypoplasia Type 6 Spinal Cord Tumor Somatoform Disorders Soft Tissue Injury Bladder Adenocarcinoma Meckel Syndrome Type 5 Muscular Dystrophy-Dystroglycanopathy Type C4 Lissencephaly due to TUBA1A Mutation Isolated Autosomal Dominant Preauricular Tag 1 Familial Temporal Lobe Epilepsy Type 3 Gastrointestinal Hemorrhage Familial Temporal Lobe Epilepsy Type 4 Upper Gastrointestinal Bleeding Familial Febrile Seizures Type 9 Adult Primary Lateral Sclerosis Skin Neoplasm Cholestasis Lymphadenitis Infant Acute Respiratory Distress Syndrome Severe Neonatal-Onset Encephalopathy with Microcephaly Strain of Adductor Muscle and Tendon X-Linked Syndromic Mental Retardation Type 13 Spinocerebellar Ataxia Type 10 Hashimoto Thyroiditis Gaucher Disease Type 1 Neonatal Hypoglycemia Dihydropyrimidine Dehydrogenase Deficiency Systemic Scleroderma Familial Teutschlaender Disease Neuronal Ceroid Lipofuscinosis Type 2 Limb-Girdle Muscular Dystrophy Type 2A Paroxysmal Non-Kinesigenic Dyskinesia Traumatic Rupture Addisonian Crisis Ear - Patella - Short Stature Syndrome Paroxysmal Kinesigenic Dyskinesia Griscelli Syndrome Type 2 Thanatophoric Dysplasia Type 1 Vitiligo Autosomal Recessive Juvenile Parkinson Disease Depression HIV Wasting Syndrome Hereditary Early-Onset Parkinson Disease Chronic Fatigue Syndrome Perry Syndrome Char Syndrome
