Sitemap | Symptoma 21601 to 21700 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. White, Spongy Plaques of Nasal Mucosa White Spongy Plaques on the Rectal Mucosa White Spongy Plaques on the Esophageal Mucosa White Spongy Plaques on the Vaginal Mucosa Diagnosis in the Second Decade of Life Caused by Mutation in the Kizuna Centrosomal Protein Gene Foveal Thinning Atrophic Changes of Central Macula Pigmentary Changes in the Peripheral Retina Mutation in the NR2F2 Gene Mutation in the XYLT1 Gene Doughy or Puffy Skin Toe Deformities Toe Clinodactyly Broad Feet Extra Ossification Monkey-Wrench Appearance of the Femoral Neck Multiple Dislocations of Large Joints Pre- and Postnatal Growth Retardation Mutation in the Zona Pellucida Glycoprotein 1 Gene Absence of Oocyte Zona Pellucida Mutation in the Beta Tubulin Gene Microcephaly (2.5-4 SD) Band Heterotopia White Matter Streaks Waxing and Waning Cardiomyopathy Frequent Neonatal Sudden Death Arrhythmias Detected Prenatally Mutation in the 155 kD Nucleoporin Gene Ventricular Tachyarrhythmias Inconsistent R-R Intervals Fast Atrial Rate Variable Age at Onset - 2 to 48 Years Mutation in the STUB1 Gene Mild Distal Sensory Axonal Neuropathy Lack of Secondary Sexual Characteristics Mutation in the IL21 Gene Globular Thalamus Globular Basal Ganglia Highly Variable Dysmorphic Features Prominent High Nasal Root Chewing Abnormalities Mutation in the Glutaminyl tRNA Synthetase Gene Intractable Severe Seizures Nodular Skin Lesions Impaired Signaling through the T Cell Receptor CD4+ T Cell Lymphopenia Relatively Benign Course after Acute Episodes in Childhood Urine 3-OH-Isovaleric Acid Increased and Ketonuria Urine 3-Methylcrotonylglycine Increased Urine Methylcitrate Increased Urine Propionyl Glycine Increased Urine 3-OH-Propionic Acid Increased Urine 3-OH-Butyric Acid Increased Urine Tricarboxylic Acid Intermediates Increased Mild Delayed Psychomotor Development Acute Episodic Encephalopathy Some Patients Do Not Develop Stroke Onset of Achalasia in Infancy or Early Childhood Mutation in the Soluble Guanylate Cyclase 1 Alpha 3 Gene Stenosis of the Intracranial Arteries Ischemic Stroke Only Apparent in Patients Taking Eculizumab Poor Response to the C5 Inhibitor Eculizumab Mutation in the Complement Component 5 Gene Onset of Symptoms in the Fourth to Sixth Decade of Life Peripheral Embolism Ventriculo-Atrial Regurgitation Myocardial Dysfunction No Mitral A Wave on Echocardiogram Absence of Atrial Wall Movement on Fluoroscopy Lack of Atrial Excitability Progressive Decrease in Atrial Voltage Progressive Biatrial Enlargement Onset of Seizures between 8 and 11 Months of Age Focal Discharge Some Patients Have Only Plantar Surface Involvement Mutation in the Keratin 6C Gene Splinter Hemorrhages of Nails Mild Hypertrophic Nail Changes Non-Epidermolytic Orthohyperkeratosis Clavus Formation Hyperhidrosis of Plantar Surface Plantar Blistering Mild Leukokeratosis of Buccal Bite Line Caused by Mutation in the Post-GPI Attachment to Protein 3 Gene Large, Fleshy Earlobes Defective Ossification of the Vertebral Bodies Persistent Notochordal Canal Vertical Clefting of the Vertebral Bodies Mutation in the Low Affinity Receptor IIIa for the Fc Fragment of IgG Defective NK Function in Spontaneous Cellular Cytotoxicity Numbers of NK Cells Decreased or Normal Lymphoproliferation Recurrent Infections - Particularly Herpes Viral Restrictive Syndrome Nail Dysplasia Diffuse Collagen Sclerosis Elastic Globules in Papillary Dermis Enlarged and Fragmented Elastic Fibers
