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Specific Language Impairment 1 Specific Language Impairment Type 2 Van der Woude Syndrome Multiple Epiphyseal Dysplasia Type 4 Noma Seckel Syndrome Type 2 Distal Myopathy with Anterior Tibial Onset Adrenal Insufficiency Adrenal Cortex Tumor Dehydration GLUT1 Deficiency Syndrome Adnexitis Aspiration Pneumonia Intranasal Administration Nocturnal Facio-Mandibular Myoclonus Poor Oral Hygiene Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Adjustment Disorder Cree Mental Retardation Syndrome Adenoma Night Terrors Usher Syndrome Type 1G Nephronophthisis 4 Senior-Løken Syndrome Type 3 Senior-Løken Syndrome Type 4 Anxiety Neurosis Brachydactyly Type A1B Autosomal Recessive Deafness 22 Autosomal Dominant Parkinson Disease 8 Sudden Infant Death Syndrome Multiple Epiphyseal Dysplasia Type 5 Vision Disorder Accidental Hypothermia Distal Spinal Muscular Atrophy Type 3 Hypoglycemia Congenital Disorder of Glycosylation Type 2D Balanoposthitis Anauxetic Dysplasia Impetigo Joubert Syndrome Type 4 Cellulitis Autosomal Dominant Spastic Paraplegia Type 19 Muscular Dystrophy-Dystroglycanopathy Type C5 Malnutrition Amish Lethal Microcephaly Malunited Fracture Familial Thyroid Dyshormonogenesis Type 6 HARP Syndrome Autosomal Recessive Spastic Paraplegia Type 7 Pneumonia Autoimmune Lymphoproliferative Syndrome Type 2B Cone Rod Dystrophy Type 10 Acetylcholinesterase Inhibitor Cellulitis of the Foot Fear Horizontal Gaze Palsy with Progressive Scoliosis Insomnia Isolated Focal Cortical Dysplasia Type 2 Obstipation Spinocerebellar Ataxia Type 19 Cradle Cap X-Linked Congenital Lower Limb Arthrogyrposis Microphthalmia Type Lenz HSD10 Mitochondrial Disease Abuse and Neglect Spondyloepimetaphyseal Dysplasia Type Bieganski Posttraumatic Stress Disorder X-Linked Syndromic Mental Retardation Type 11 Thrombocytopenia Roifman Syndrome Congenital Heart Disease X-Linked Syndromic Mental Retardation Type Armfield Tetralogy of Fallot X-linked Spastic Paraplegia Type 16 X-Linked Mental Retardation Type 72 Multinodular Goiter 2 Faciocardiomusculoskeletal Syndrome Type Uruguay Thrombocytopenia-Absent Radius Syndrome IMAGE Syndrome Atrial Septal Defect X-linked Severe Congenital Neutropenia Familial X-Linked Thrombocytosis Absence Seizure X-linked Mental Retardation Type Cabezas X-Linked Syndromic Mental Retardation Type Hedera Bartholin's Cyst or Abscess X-Linked Mental Retardation Type 46 Cubitus Valgus with Mental Retardation and Unusual Facies X-Linked Syndromic Mental Retardation Type 28 X-Linked Mental Retardation with Cerebellar Hypoplasia and Distinctive Facial Appearance X-linked Distal Spinal Muscular Atrophy Type 3 Pleural Effusion Payr's Syndrome X-Linked Syndromic Mental Retardation Type Claes-Jensen Nephrogenic Syndrome of Inappropriate Antidiuresis Pleuritic Pain X-Linked Recessive Hypophosphatemic Rickets Dent Disease Type 2 Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency Septicemia