15301 to 15400 most common queries

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

• Brachydactyly Type B2
• Autosomal Recessive Spastic Ataxia with Leukoencephalopathy
• Gastric Dilatation
• Spinal Cord Tumor
• Somatoform Disorders
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2M
• Lissencephaly due to TUBA1A Mutation
• Isolated Autosomal Dominant Preauricular Tag 1
• Familial Febrile Convulsions 9
• Skin Neoplasm
• Infant Acute Respiratory Distress Syndrome
• Strain of Adductor Muscle and Tendon
• Spinocerebellar Ataxia Type 10
• Familial Teutschlaender Disease
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2A
• Paroxysmal Non-Kinesigenic Dyskinesia
• Traumatic Rupture
• Griscelli Syndrome Type 2
• Perry Syndrome
• Char Syndrome
• Patterson Pseudoleprechaunism Syndrome
• Adult-Onset Autosomal Dominant Leukodystrophy
• Facioauriculoradial Dysplasia
• Orofaciodigital Syndrome, Type 5
• Postaxial Oligodactyly, Tetramelic
• Long QT Syndrome 5
• Infantile Hypertrophic Pyloric Stenosis 1
• Retinitis Pigmentosa 9
• Ulnar Mammary Syndrome
• Polyneuritis
• Autosomal Dominant Spastic Paraplegia Type 4
• Poisoning
• Distal Hereditary Motor Neuropathy Type 1
• Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome
• Spondyloepiphyseal Dysplasia Type MacDermot
• Addictive Behavior
• Steatocystoma Multiplex With Natal Teeth
• Physical Exertion
• Phlegmon
• Spondyloepimetaphyseal Dysplasia - Abnormal Dentition Syndrome
• Suicidal Depression
• Infantile 3-Phosphoglycerate Dehydrogenase Deficiency
• Papilloma
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2G
• Odonto Tricho Ungual Digito Palmar Syndrome
• Oto-Facio-Osseous Gonadal Syndrome
• Primary Hypomagnesemia with Secondary Hypocalcemia
• Pure Hair-Nail Ectodermal Dysplasia
• Acyclovir
• Viremia
• Nephronophthisis 2
• Spondyloepimetaphyseal Dysplasia Type Missouri
• Ventriculomegaly with Defects of the Radius and Kidney
• Progeroid Facial Appearance with Hand Anomalies
• Habrodysplasia
• Acute Respiratory Acidosis
• Familial Hemiplegic Migraine Type 2
• Bartter Syndrome
• Early-Onset Generalized Torsion Dystonia
• Spondyloepimetaphyseal Dysplasia Type Shohat
• Congenital Disorder of Glycosylation Type 1B
• Progressive Epilepsy-Intellectual Disability Syndrome, Type Finnish
• Ingrown Nail
• Spondyloepimetaphyseal Dysplasia Type Geneviève
• Familial Normophosphatemic Tumoral Calcinosis
• Camptodactyly - Tall Stature - Scoliosis - Hearing Loss
• Familial Isolated Arrhythmogenic Right Ventricular Dysplasia Type 11
• Primary Pigmented Nodular Adrenocortical Disease 1
• Acute Inflammation
• Combined Oxidative Phosphorylation Deficiency Type 3
• Acute Infectious Disease
• Holoprosencephaly Type 5
• Autosomal Recessive Deafness 42
• Autosomal Recessive Deafness 46
• Short Stature and Facio-Auriculo-Thoracic Malformations
• Singh-Williams-McAlister Syndrome
• Microphthalmia Syndromic 6
• Neuronal Ceroid Lipofuscinosis 4
• Autosomal Dominant Progressive External Ophthalmoplegia Type 4
• Hypomyelination - Congenital Cataract
• Maxillary Neoplasm
• Drotrecogin Alfa
• Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 2
• Malignant Gastric Neoplasm
• Limb-Mammary Syndrome
• Autosomal Dominant Spastic Paraplegia Type 8
• ACHOO Syndrome
• Biliary Cirrhosis
• Alopecia Areata Type 1
• Amyotrophic Lateral Sclerosis 1
• Spastic Ataxia with Congenital Miosis
• Brachydactyly Type A1
• Brachydactyly Type A6
• Langer Nishino Yamaguchi Syndrome
• Idiopathic Childhood-Onset Basal Ganglia Calcification
• Wellesley Carmen French Syndrome
• Vertebral Osteomyelitis
• Gastroduodenal Fistula
• Charcot-Marie-Tooth Disease Type 2A1
• Familial Cluster Headache