44701 to 44800 most common queries

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

• Non-Scarring Skin Blistering
• Allelic to Hand Osteoarthritis
• Pulmonary Valve - Mild Stenosis
• Defects in Visual Cue Processing
• Artefact - Patient Movement
• Pronounced Convex Arch of Eyebrows
• Abnormal Tonometry
• Impaired Lipolysis
• Caused by Mutations in the Parkin Gene (PARK2)
• Pulmonary Vascular Resistance Increased
• Arthrogryposis
• Mild Finger Contractures
• Caused by Mutation in the Peripherin 2 Gene
• Mutation in the Coagulation Factor VII Gene
• Dermatitis Infectious due to Immunodeficiency and Impetigo
• Posterior Fossa Abnormalities
• Allelic to MATN-3 Related Spondyloepimetaphyseal Dysplasia
• Upper Limb Sensory Loss May Occur Later
• Moderate Aortic Regurgitation
• Artefact - Technical Problems
• Defects in Auditory Cue Processing
• Photosensitivity
• Characteristic Backward Head Tilt
• Small Adipocytes
• No Lewy Bodies
• Severely to Profoundly Delayed Psychomotor Development
• Normal Color Vision
• Poor Visual Tracking
• Trinucleotide Repeat Expansion in the TBP Gene
• Mutation in the LAMC2 Gene
• NADPH Oxidase Activity Decreased
• Mild Stenosis - Aortic Valve
• Mutation in the Plectin Gene
• Possibly Restrictive Pattern in Pulmonary Function Tests
• Upper Limb Weakness May Occur Later
• Increased Hair Growth
• Focal Pattern
• Caused by Mutation in the Enolase 3 Gene
• Normal Breast Development
• Heterozygous Carriers Have an Increased Risk of Metabolic Dysfunction
• Cuneiform Opacities in Lens Periphery
• Neuronal Loss in the Locus Ceruleus
• Hyperfluorescent Ring in Area of Macular Lesions (FA)
• Cortical Visual Impairment
• Caused by Mutation in the Beta-3-Laminin Gene
• Velocity of Larger Saccades Increased
• Hypoplastic Hemidesmosomes
• Deficiency or Absence of P22-Phox Protein
• Moderate Tricuspid Regurgitation
• Mutations in the SLC4A4 Gene
• Mutations in the PITX2 Gene
• Focal Continuous Abnormality
• Enolase 3 Activity Decreased
• Estrogen and Progesterone Low
• Red Urine
• Mutation in the Hormone Sensitive Lipase Gene
• Blue-White Dots Throughout Lens More Numerous in Cortex
• Mutation in the LAMA3 Gene
• Arden Ratios Normal or Decreased (Electrooculography)
• Neuronal Loss and Gliosis in the Substantia Nigra Pars Compacta
• Overshooting Horizontal Saccades
• Negative Staining with HD121
• Cerebral White Matter Decreased
• Tricuspid Valve - Thickening to Severe Stenosis
• Deficiency or Absence of Cytochrome B
• Red Cell Osmotic Resistance Increased
• Multifocal Independent Spikes
• Skin Tear
• Iris Dysplasia (Goniodysgenesis)
• Symptoms Induced by Strenuous Exercise
• Mutation in the Collagen XVII Alpha 1 Polypeptide Gene
• Abnormal Fat Accumulation in the Clavicular Regions
• Increased Pigmented Nevi
• Cone and Rod Responses on ERG Normal or Decreased
• No Dementia
• Concave Nails (4th and 5th Digits)
• Relative Preservation of the Cerebellar Folia
• Minimal or Absent Scarring
• Allelic to Dyggve-Melchior-Clausen Disease
• Mild to Moderate Mitral Regurgitation
• Biopsy: Lipid-Laden Macrophages
• Normal Distal Tubule Acid Excretion
• Generalized Asynchronous Slow-Waves
• Mutation in the LDHA Gene
• Carcinoma of the Vulva
• Mutations in the PMP22 Gene
• Diagnosis Occurs between 23 and 33 Weeks' Gestation
• Variable Shortening of Metatarsals IV and V
• Stellate Retinal Folds
• Abnormal Fat Accumulation in the Labia Majora
• Diurnal Fluctuations of Symptoms
• Carpal Bone Development Advanced Over That of Other Hand Bones
• Mitral Valve - Thickening to Severe Stenosis
• Neonatal-Onset Generalized Blistering
• Involuntary, Repetitive Movements
• Sagittal Vertebral Cleft
• Bicarbonate Wasting Renal Tubular Acidosis
• Abscess Formation in Any Organ
• Bisynchronous Slow-Waves
• Spinal Cord Concussion