15501 to 15600 most common queries

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

• Acne Varioliformis
• Methylmalonic Aciduria Type cblA
• Microcephaly with Spastic Quadriplegia
• Isolated Succinate-CoQ Reductase Deficiency
• Molybdenum Cofactor Deficiency Type B
• Molybdenum Cofactor Deficiency Type A
• Mucus Inspissation of Respiratory Tract
• Lethal Multiple Pterygium Syndrome
• Autosomal Recessive Spastic Paraplegia Type 14
• Mesomelic Dysplasia, Savarirayan Type
• Autosomal Dominant Spastic Paraplegia Type 13
• Charcot-Marie-Tooth Disease Type 4G
• Frontoocular Syndrome
• Amish Nemaline Myopathy
• Dentinogenesis Imperfecta Type 1 with Autosomal Dominant Deafness 39
• Late-Onset Retinal Degeneration
• Distal Hereditary Motor Neuropathy Type Jerash
• Confusion
• Citrullinemia Type 2, Neonatal Onset
• Multifocal Atrial Tachycardia
• Autism Related Speech Delay
• Charcot-Marie-Tooth Disease Type 2C
• Acidifying Agent Poisoning
• Acid Base Disorder
• Chromosome 22q13.3 Deletion Syndrome
• Generalized Motor Seizure
• Developmental Disabilities
• Juvenile Primary Lateral Sclerosis
• Charcoal
• Generalized Epilepsy with Febrile Seizures-plus Type 4
• Cerebrovascular Disorder
• Lysosomal Acid Phosphatase Deficiency
• Autosomal Dominant Spastic Paraplegia 33
• Spinocerebellar Ataxia Type 23
• Carotid Artery Thrombosis
• Autosomal Dominant Spastic Paraplegia Type 31
• Cold-Induced Sweating Syndrome Type 2
• Rhizomelic Dysplasia - Scoliosis - Retinitis Pigmentosa
• Holoprosencephaly - Recurrent Infections - Monocytosis
• Nemaline Myopathy 7
• Joubert Syndrome
• Autosomal Dominant Classic Optic Atrophy
• Nephrotic Syndrome Type 3
• Cerebrooculofacioskeletal Syndrome Type 4
• Renal Coloboma Syndrome
• Cornea Guttata with Anterior Polar Cataracts
• Craniosynostosis
• Achondrogenesis Type 2
• Achondrogenesis Type 1B
• Dwarfism Levi Type
• Microcytic Anemia
• Neuhauser Eichner Opitz Syndrome
• Epiblepharon of Lower Lid
• Transient Bullous Dermolysis of the Newborn
• Familial Thoracic Aortic Aneurysm 4
• Autosomal Dominant Familial Exudative Vitreoretinopathy
• Bladder Neoplasm
• Bismuth
• Secondary Amenorrhea
• Anovulatory Cycle
• Intrathoracic Gastric Volvulus
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2B
• Lethal Muscular Hypertonia
• Congenital Myasthenic Syndrome Type 1B
• Autosomal Recessive Myeloproliferative Disease
• Myopathy with Giant Abnormal Mitochondria
• Esophageal Candidiasis
• Multicore Myopathy
• Visual Impairment
• Chagas Disease
• Nakajo Syndrome
• Neuronal Ceroid Lipofuscinosis 10
• Hereditary Sensory and Autonomic Neuropathy with Spastic Paraplegia
• Esophageal Metastasis
• Ophthalmoplegia totalis with Ptosis and Miosis
• Autosomal Recessive Progressive External Ophthalmoplegia
• Autosomal Recessive Isolated Optic Atrophy
• Osteogenesis Imperfecta Type 2
• Chemical Pneumonitis
• Autosomal Recessive Distal Osteolysis Syndrome
• Autosomal Recessive Osteopetrosis Type 1
• Pelizaeus-Merzbacher-Like Disease Type 2
• Pelviscapular Dysplasia
• Achromatopsia 3
• Acetohexamide
• Erectile Dysfunction
• Peroxisomal ACYL-COA Oxidase Deficiency
• Acrootoocular Syndrome
• Hunger
• Pygmy (Disorder)
• Knobloch Syndrome Type 1
• Acetazolamide
• Acetanilid Poisoning
• Autosomal Recessive Spastic Ataxia Type Charlevoix-Saguenay
• Autosomal Recessive Spinocerebellar Ataxia 3
• Brachyolmia, Recessive Hobaek Type
• Spondylocarpotarsal Synostosis
• Aneurysm
• Chronic Active Hepatitis
• Taurodontia Absent Teeth Sparse Hair