15901 to 16000 most common queries

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

• Oculopalatoskeletal Syndrome
• Malpuech Syndrome
• Lethal Ataxia with Deafness and Optic Atrophy
• Autosomal Recessive Spastic Paraplegia Type 23
• Carpenter-Waziri Syndrome
• Jackson Weiss Syndrome
• Familial Infantile Bilateral Striatal Necrosis
• Andermann Syndrome
• Onat Syndrome
• Digitorenocerebral Syndrome
• Hypertrichotic Osteochondrodysplasia
• Spinocerebellar Ataxia Type 4
• Spinocerebellar Ataxia, Type 2
• Slow-Channel Congenital Myasthenic Syndrome
• Action Myoclonus - Renal Failure Syndrome
• Short Sleeper
• Emery-Dreifuss Muscular Dystrophy Type 1
• Scapuloperoneal Spinal Muscular Atrophy
• Classic Homocystinuria
• FRAXE Intellectual Disability
• Early Infantile Epileptic Encephalopathy Type 6
• Reynolds Syndrome
• Multiple Self-Healing Squamous Epithelioma
• Hereditary Neutrophilia
• Book's Syndrome
• Curry Hall Syndrome
• Uncombable Hair Syndrome
• Mandibuloacral Dysostosis
• Dermochondrocorneal Dystrophy
• Congenital Generalized Fibromatosis
• Kyphomelic Dysplasia
• Cranioectodermal Dysplasia
• Metaphyseal Chondrodysplasia, Spahr Type
• Spondyloepimetaphyseal Dysplasia Type Irapa
• Dyssegmental Dysplasia Type Rolland-Desbuquois
• Schneckenbecken Dysplasia
• Myopathy with Abnormal Lipid Metabolism
• Autosomal Recessive Centronuclear Myopathy
• Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2
• Congenital Muscular Dystrophy Type Ullrich
• Fukuyama Muscular Dystrophy
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2C
• Reticulate Acropigmentation of Kitamura
• Kohlschütter-Tönz Syndrome
• Hereditary Benign Telangiectasia
• Nephrotic Syndrome Type 1
• Factor H Deficiency
• Recurrent Neisseria Infections due to Factor D Deficiency
• Thromboxane Synthetase Deficiency
• Myeloperoxidase Deficiency
• X-Linked Charcot-Marie-Tooth Disease Type 1
• Hereditary Motor and Sensory Neuropathy Type 6
• Chorea Acanthocytosis Syndrome
• Autosomal Recessive Spastic Paraplegia Type 20
• Spinal Muscular Atrophy Type 2
• Roberts Syndrome
• Tietz Syndrome
• Birt-Hogg-Dubé Syndrome
• Deficiency of Interleukin-36-Receptor Antagonist
• Fish-Eye Disease
• Dihydropyrimidinuria
• Cytosolic Acetoacetyl-CoA Thiolase Deficiency
• 3-Methylglutaconic Aciduria
• Dopamine Beta-Hydroxylase Deficiency
• Familial Candidiasis Type 4
• Frontotemporal Dementia
• Aplasia Cutis Congenita
• Hunermann Conradi Syndrome
• Otolith
• Osteosarcoma
• Gastric Volvulus
• Osteomyelitis of the Frontal Bone
• Ganser Syndrome
• Osteogenesis Imperfecta Type 3
• Froehlich's Syndrome
• Osteogenesis Imperfecta
• Francisella Tularensis
• Organic Delusional Syndrome
• Fort Bragg Fever
• Orbital Emphysema
• Foreign Body in the Pharynx
• Oral Candidiasis
• Oophoritis
• Folliculitis Decalvans
• Onycholysis
• Follicular Thyroid Carcinoma
• Olivopontocerebellar Atrophy
• Focal Seizure
• Old Age
• Fitzsimmons-McLachlan-Gilbert Syndrome
• Obstruction of the Lung
• Fibular Aplasia-Tibial Campomelia-Oligosyndactyly Syndrome
• Obesity
• Fibromuscular Dysplasia
• Normochromic Anemia
• Fetal Akinesia - Cerebral and Retinal Hemorrhage Syndrome
• Non-24 Hour Sleep-Wake Disorder
• Femoral Neck Stress Fracture
• Nocturnal Facio-Mandibular Myoclonus
• Femoral Hypoplasia