44501 to 44600 most common queries

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

• Urine Thiosulphate Increased
• Allelic to Acrocapitofemoral Dysplasia
• Periosteal Hyperostosis of Knee
• Left Sided Liver
• Distinct Disorder from Marinesco Sjogren Syndrome
• Round Ilium
• Background Activity Abnormal
• Deletion of 11q23
• Onset within First Year of Life
• Mutation in the Serologically Defined Colon Cancer Antigen 8 Gene
• Rapid Progression
• Mixed Cerebellar - Pseudobulbar Dysarthria
• Mild Proptosis
• Relative Resting Bradycardia
• Clinical and Biochemical Abnormalities Disappear with Age
• Aseptic Necrosis of Head of Humerus
• Mutation in the TFAP2A Gene
• Progressive Thickening and Furrowing of Facial Skin
• Increased Urinary Isobutyryl Glycine
• Anterior Flattening and-or Beaking of Vertebrae
• Awake Beta Activities Excessively Fast
• Developmental Delay - Variable Severity
• Prevalent in Bulgarian Gypsies
• See Also Two X-Linked Forms
• Aseptic Necrosis of Head of Femur
• Mutation in the Prion Protein Gene
• Caused by Mutation in the Thioredoxin-Like 4A Gene
• Recurrent/Chronic Respiratory Infections
• Aneurysm of Right Middle Cerebral Artery, Horizontal Segment
• Wide Clinical Variability
• Cerebrospinal Fluid Interferon-Alpha Increased
• Fasting Ketosis
• Mutation in the NK2 Homeobox 5 Gene
• Caused by Mutation in the Eyes Absent 1 Gene (EYA1)
• Cytochrome C Oxidase Deficiency in Skeletal Muscle and Brain
• Brainstem May Show Neuronal Loss
• Unilateral Renal Agenesis
• Bilateral Choanal Atresia or Choanal Stenosis
• Short Limb - Short Stature - Childhood Onset
• Abnormal Corticomedullary Differentiation
• Oral Contraceptives May Also Cause Symptoms
• Slowing - Theta Waves Unilaterally Left
• Neuropathy Becomes Apparent in Childhood
• Capillary Tortuosity in Nail Beds
• Complication of Corneal Transplant
• Mild Elevation of Triglycerides
• Abnormal Pulmonary Venous Return to Right Atria
• Alpha Interferon Increased
• Abnormal Electrooculogram EOG
• Aplasia or Stenosis of Lacrimal Duct
• Thalamic Neuronal Loss especially in the Medial Dorsal Nucleus
• Mutation in the Transportin 3 Gene
• Vaginal Agenesis
• Fasting Triglycerides Elevated
• Slowing - Theta Waves Bilaterally
• Mutation in the TMEM231 Gene
• Ceruloplasmin Decreased
• Basement Membrane Abnormally Spread in Vascular Smooth Muscle Cells
• Medial Calcification of Medium-Sized and Major Arteries
• Limited Clinical Information for MKS1 Mutations (as of October 2014)
• Mild Elevation of Cholesterol
• Thickening of Perioral Tissues
• No Evidence of Common Prenatal Infections
• Sinus Venosus Type Atrial Septal Defect
• Impaired Thermal Sense
• Septate Vagina
• Nasopharyngeal Hairy Polyp
• Progressive Sleep Impairment
• Paroxysmal Activity - Spikes Temporal Right
• Increased Mitochondria with Rare Paracrystalline Inclusions
• Renal Cysts
• Yellowish Lip - Mucosal Nodules
• Microtia
• Dermal Arteriole Dissociation in Vascular Smooth Muscle Cells
• Loud Snoring
• Mild Elevation of Transaminases
• One Family Reported (as of October 2014)
• Sparing of the Inferior Olives
• Axonal Degeneration in Older Patients
• Atrial Septal Defect Type Secundum
• Tetraplegic Spasticity
• Cleft of Cervical and Dorsal Vertebral Bodies
• Uterus Didelphys
• Refractory Insomnia
• MRI Scan showing Molar Tooth Sign
• Abnormal Z Bands
• Salmon Spots
• Paroxysmal Activity - Spikes Parietal
• Variable Hypoglycemia
• Mutation in the Tripartite Motif Containing Protein 32 Gene
• Automatic Behavior
• Glomerular Basement Membrane Normal
• Therapy-Induced Dyskinesias
• Mild Loss of Neurons in the Cerebellum
• Nerve Biopsy Shows Hypomyelination
• Profound Developmental Retardation
• Partial Synostosis between the Atlas and the Base of the Occiput
• Rastelli Type A Endocardial Cushion Defect
• Good Response to Vitamin D Treatment
• Filamentous Inclusions in Muscle Fibers