Sitemap | Symptoma 22801 to 22900 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Possible Increased Risk of Germ-Cell Tumors Small or Undeveloped Breasts Ovarian Cancer Streak Ovaries on Ultrasound Large Optic Discs Bilateral Ureteral Aplasia Bilateral Renal Aplasia Frequently Fatal within the First Year of Life C-Peptide Low or Undetectable Anteriorly Placed Anus Mutation in the EDN1 Gene Dilation of Vein of Galen Thickened Zygomatic Process of Right Temporal Bone Submucosal Velar Cleft Lingual Appendages Ectopic Uvula Bilateral Conductive Hearing Loss Mutation in the KIAA0226 Gene Age of Onset: 18-53 Years Small Horn Cysts Pronounced Hyperpigmentation at Tips of Rete Ridges Digitiform Acanthosis of the Rete Ridges Small Vessel Disease Perivascular T Lymphocytes Interstitial Neutrophils and Macrophages Vasculitis in the Reticular Dermis Lupus Anticoagulant Acute-Phase Reactants during Fever Ischemic Digital Necrosis Neurologic Sequelae of Stroke Brownish-Black Macules on Dorsa of Hands and Feet Spotted and Reticulate Pigmentation of Flexural Areas of Skin Mutation in the LZTR1 Gene Prominent Subnasal Region Progressive Optic Nerve Atrophy Small, Atonic Pupils Broad Dense Laterally Descending Eyebrows Widened Lateral Ventricles Speech Severely Limited or Absent Postnatal Development of Hypertonic Extremities Congenital Axial or Generalized Hypotonia Mutation in the TRK Fused Gene Mild Sensory Impairment Normal Early Developmental Milestones Age of Onset from 18 to 45 Years No Vestibular Dysfunction Post-Lingual Bilateral Progressive Hearing Loss Variable Clinical Features Two Peaks of Onset - Childhood and Adult Mutation in the Chloride Channel 2 Gene Chorioretinopathy Myelin Microvacuolation Diffuse Hyperintensities in the White Matter in Children Low Apparent Diffusion Coefficients Older Individuals Had Moderate to Severe Hearing Loss Age of Onset 5 to 40 Years Vertigo - Single Occurrence Loss of Independent Ambulation in Second Decade Gait Difficulties and Beginning of Cognitive Decline in First Decade Onset in Early Childhood after Initially Normal Development Mutation in the COASY Gene Hypointensities in the Basal Ganglia (T2-Weighted) Iron Accumulation in the Basal Ganglia Seen on MRI Normal Initial Psychomotor Development Reported in the Ohio Amish Anabaptist Community Caused by Mutation in the Kaptin Gene (KPTN) Macrocephaly (3-5 SD) Mutation in the CSPP1 Gene Single Nostril Anophthalmia Fused Eyes Short, Horizontal Ribs Hyperechogenic Kidneys Elongated Superior Cerebellar Peduncles Dysplastic Superior Cerebellar Vermis Mild Bowing of Humeri and Femora Irregular Sciatic Notches Trident Acetabulum with Spurs Dilated Calyces Caused by Mutation in the Atlastin GTPase 3 Gene Impaired Bone Healing Chronic Ulceration due to Sensory Neuropathy Bone Destruction Anemia Does Not Respond to Alpha Interferon Treatment Anemia Is Transfusion-Dependent Erythroid Hyperplasia Seen on Bone Marrow Biopsy Metatarsal Duplication Hypoplasia of Terminal Phalanges Abnormal Phalanges Chronic Respiratory Distress Trident Acetabulum Early Cystic Dysplasia Mild Structural Abnormalities End Stage Renal Disease by Third Decade of Life Mild Ventriculomegaly Onset between 8 and 30 Years Mutation in the Tenascin C Gene Postlingual Progressive Sensorineural Hearing Loss Sphincter Dysfunction Vibratory Sense at the Ankles Decreased
