11901 to 12000 most common queries

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

• Usher Syndrome Type 2
• Epidermolysis Bullosa Simplex
• Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect
• Congenital Adrenal Hyperplasia
• Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency
• Classic Congenital Adrenal Hyperplasia
• Congenital Adrenal Hyperplasia due to 3-Beta-Hydroxysteroid Dehydrogenase Deficiency
• Congenital Lipoid Adrenal Hyperplasia
• Osteogenesis Imperfecta Typ 4
• Myopic Macular Degeneration
• Primary Cutaneous Marginal Zone B-Cell Lymphoma
• Inflammatory Myofibroblastic Tumor
• Aromatase excess syndrome
• Autosomal Recessive Osteopetrosis Type 7
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2D
• Autosomal Dominant Non-Syndromic Mental Retardation
• Autosomal Dominant Non-Syndromic Intellectual Disability
• Nivelon-Nivelon-Mabille Syndrome
• Tracheal Agenesis
• Bleeding Diathesis due to a Collagen Receptor Defect
• Familial Porencephaly
• Primary Cutaneous B-Cell Lymphoma
• Cerebro-Oculo-Facio-Skeletal Syndrome 1
• Familial Juvenile Hypertrophy of the Breast
• Non-Neuropathic Heredofamilial Amyloidosis
• Nonsyndromic Isolated Dilated Cardiomyopathy
• Familial Isolated Dilated Cardiomyopathy
• Uterine Cervical Aplasia and Agenesis
• X-Linked Recessive Ocular Albinism
• Alzheimer Disease 8
• Early-Onset Autosomal Dominant Alzheimer Disease
• Bicornuate Uterus
• Bicervical Bicornuate Uterus and Blind Hemivagina
• Short Rib-Polydactyly Syndrome
• Muir-Torre Syndrome
• Mixed Germ Cell Tumor
• Congenital Pulmonary Lymphangiectasia
• Malignant Vaginal Neoplasm
• Acral Peeling Skin Syndrome
• Polyembryoma
• Foveal Hypoplasia - Presenile Cataract Syndrome
• Isolated Congenital Breast Hypoplasia or Aplasia
• Pseudo-Zellweger Syndrome
• 46,XX Disorder of Sex Development
• Disorder of Sex Development - Intellectual Disability Syndrome
• Familial Spontaneous Pneumothorax
• Autosomal Recessive Osteopetrosis Type 3
• Thanatophoric Dysplasia 2
• Bilateral Multicystic Dysplastic Kidney
• Adult-Onset Cervical Dystonia Type DYT23
• Congenital Enterovirus Infection
• Congenital Fiber-Type Disproportion Myopathy
• Galactosialidosis
• Congenital Diaphragmatic Hernia Type 3
• Anterior Diaphragmatic Hernia
• Congenital Diaphragmatic Hernia Type 2
• Craniosynostosis-Dandy-Walker Malformation-Hydrocephalus Syndrome
• Biotinidase Deficiency
• D-Glyceric Aciduria
• Molybdenum Cofactor Deficiency Type C
• Brosnan Syndrome
• 46,XX Gonadal Dysgenesis
• Neurogenic Arthrogryposis Multiplex Congenita
• Erdheim-Chester Disease
• 46,XY Gonadal Dysgenesis - Motor and Sensory Neuropathy Syndrome
• Acromesomelic Dysplasia Type Maroteaux
• Arthrogryposis due to Muscular Dystrophy
• Seborrhea-Like Dermatitis with Psoriasiform Elements
• Congenital Enteropathy due to Enteropeptidase Deficiency
• Aromatase Deficiency
• Familial Candidiasis Type 6
• Immunodeficiency Type 51
• Monocyte Chemotactic Disorder
• Lymphokine Deficiency
• Familial Candidiasis Type 1
• Candidiasis of Skin and Nails
• Hereditary North American Indian Childhood Cirrhosis
• Familial Scaphocephaly Syndrome Type McGillivray
• Autosomal Dominant Coarctation of Aorta
• Autosomal Dominant Macrothrombocytopenia
• Acro-Pectoral Syndrome
• Congenital Deficiency in Alpha-fetoprotein
• Hereditary Persistence of Alpha-Fetoprotein
• Tetrasomy X
• Adenine Phosphoribosyl Transferase Deficiency
• Combined Oxidative Phosphorylation Defect Type 14
• Waters-West Syndrome
• Mucocutaneous Venous Malformations
• Gigantism - Acromegaly
• Neonatal Adrenoleukodystrophy
• Infantile Refsum Disease
• Familial Scaphocephaly Syndrome
• Immuno-Osseous Dysplasia
• X-Linked Centronuclear Myopathy
• Classic Galactosemia
• Recurrent Infection due to Specific Granule Deficiency
• Neurodegeneration with Brain Iron Accumulation
• T-B+ Severe Combined Immunodeficiency due to CD3zeta
• Immunodeficiency due to a C5 to C9 Complement Component Deficiency
• Refsum Disease Type 2