11101 to 11200 most common queries

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

• Familial Pseudohyperkalemia
• Bacterial Sepsis of Newborn
• Sepsis of Newborn due to Other and Unspecified Streptococci
• Sepsis in Premature Infants
• Partial Deep Dermal and Full Thickness Burns
• Mitochondrial Disease
• Peroxisomal Disease
• Rare Inborn Errors of Metabolism
• Hereditary Persistence of Fetal Hemoglobin
• Incessant Infant Ventricular Tachycardia
• Generalized Arterial Calcification of Infancy
• Keratolytic Winter Erythema
• Familial Short QT Syndrome
• Torsade-De-Pointes Syndrome with Short Coupling Interval
• Malignant Mesothelioma
• Lethal Arthrogryposis - Anterior Horn Cell Disease Syndrome
• Distal Hereditary Motor Neuropathy
• Posterior Cortical Atrophy
• Hereditary Geniospasm
• Congenital Lactase Deficiency
• Isolated Follicle Stimulating Hormone Deficiency
• Systemic Vasculitis
• Familial Cutaneous Collagenoma
• Corneal Dystrophies
• Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia
• Idiopathic Disseminated Cytomegalovirus Infection
• Idiopathic Recurrent and Disabling Cutaneous Herpes
• Combined Deficiency of Factor V and Factor VIII Type 2
• Combined Deficiency of Factors V and VIII with Normal Protein C and Protein C Inhibitor
• Combined Deficiency of Factors V and VIII
• Familial Vascular Leukoencephalopathy
• Epidermal Nevus Syndrome
• Mitochondrial DNA Depletion Syndrome
• Madelung Deformity
• Bietti Crystalline Dystrophy
• Uveal Melanoma
• Acute graft versus host disease
• Müllerian Aplasia
• Retinal Dystrophy
• Psychogenic Movement Disorders
• Familial Isolated Restrictive Cardiomyopathy
• Intestinal Lymphangiectasia
• Cystoid Macular Dystrophy
• Progressive Bifocal Chorioretinal Atrophy
• North Carolina Macular Dystrophy
• Majeed Syndrome
• Syndromic Microphthalmia Type 10
• Acute Interstitial Pneumonia
• Hepatic Veno-Occlusive Disease-Immunodeficiency Syndrome
• Grange Syndrome
• Eiken Syndrome
• Familial Reactive Perforating Collagenosis
• Elastosis perforans serpiginosa
• Disorder of Purine Metabolism
• Disorder of Glycerol Metabolism
• Crigler-Najjar Syndrome Type 2
• Hereditary Hypotrichosis Simplex
• Atrichia with Papular Lesions
• X-Linked Membranoproliferative Glomerulonephritis
• Sarcocystosis
• McLeod Neuroacanthocytosis Syndrome
• Gestational Trophoblastic Neoplasm
• Idiopathic Bronchiectasis
• Linear IgA Dermatosis
• Recurrent Acute Pancreatitis
• Pulmonary Blastoma
• Benign Recurrent Intrahepatic Cholestasis
• Isolated Partial Vaginal Agenesis
• Congenital Pseudoarthrosis of Clavicle
• Nephrotic Syndrome with Minimal Changes
• Anhidrotic Ectodermal Dysplasia - Immunodeficiency - Osteopetrosis - Lymphedema Syndrome
• Anonychia with Flexural Pigmentation
• Athabaskan Brainstem Dysgenesis Syndrome
• Meconium Aspiration Syndrome
• Posttransplant Lymphoproliferative Disease
• Bronchopulmonary Dysplasia
• Retinal Cavernous Hemangioma
• Hypoalphalipoproteinemia
• Nocardiosis
• Rat-Bite Fever
• Junctional Epidermolysis Bullosa
• Familial Cylindromatosis
• Dyschromatosis Universalis Hereditaria
• Hyperkeratosis Lenticularis Perstans
• Proliferating Trichilemmal Cyst
• Acquired Hypertrichosis Lanuginosa
• Hereditary Hypotrichosis Type Marie Unna
• Familial Atrial Myxoma
• Familial Atrial Fibrillation
• Pulmonary Branch Stenosis
• Congenital Mitral Stenosis
• Adrenal Incidentaloma
• Reflex Epilepsy
• Fetal and Neonatal Alloimmune Thrombocytopenia
• Familial Keratoacanthoma
• Hereditary Leiomyomatosis and Renal Cell Cancer
• Peeling Skin Syndrome
• Hypogonadotropic Hypogonadism Type 7
• Heterotaxia
• Echinococcus Granulosus Infection