14701 to 14800 most common queries

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

• Familial Episodic Pain Syndrome 2
• Hereditary Sensory and Autonomic Neuropathy Type 7
• Musculocontractural Ehlers-Danlos Syndrome Type 2
• Early-Onset Parkinson Disease 20
• Atypical Juvenile Parkinsonism
• Primary Ciliary Dyskinesia 25
• Early Infantile Epileptic Encephalopathy Type 18
• Early Infantile Epileptic Encephalopathy Type 17
• Primary Ciliary Dyskinesia 23
• Primary Ciliary Dyskinesia 22
• Tenosynovitis
• Catecholaminergic Polymorphic Ventricular Tachycardia 5
• Age-Related Macular Degeneration 13
• Familial Thoracic Aortic Aneurysm 8
• Retinitis Pigmentosa with Situs Inversus
• Hereditary Factor II Deficiency
• Specific Language Impairment 5
• Autosomal Dominant Myopia 22
• Edema
• Nephrogenic Diabetes Insipidus
• Autosomal Recessive Primary Microcephaly 11
• Cortical Dysplasia Complex with other Brain Malformations 4
• Cortical Dysplasia Complex with other Brain Malformations 3
• Primary Amyloidosis
• Familial Amyloid Polyneuropathy
• Multiple Congenital Anomalies - Hypotonia - Seizures Type 3
• Hepatosplenic Amyloidosis
• Cutaneous Amyloidosis
• Nephronophthisis 16
• Myeloma-associated Amyloidosis
• Childhood-Onset Epileptic Encephalopathy
• Amyloidosis in Familial Mediterranean Fever
• Limb-Girdle Muscular Dystrophy Type 2S, Autosomal Recessive
• Muscle-Eye-Brain Disease Type A14
• Central Precocious Puberty Type 2
• Idiopathic Familial Pulmonary Arterial Hypertension
• Early Infantile Epileptic Encephalopathy Type 16
• Multiple Mitochondrial Dysfunctions Syndrome Type 3
• Amprenavir
• Toxic Hemolytic Anemia
• Dowling-Degos Disease Type 1
• Ampicillin-Sulbactam
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2R
• Perrault Syndrome Type 4
• Ampicillin
• Infantile Myofibromatosis
• Amphotericin B
• Congenital Neutropenia - Myelofibrosis - Nephromegaly Syndrome
• Complex Cortical Dysplasia with other Brain Malformations 2
• Bruxism
• Hypogonadotropic Hypogonadism Type 21
• Hypogonadotropic Hypogonadism Type 20
• Hypogonadotropic Hypogonadism Type 19 with or without Anosmia
• Hypogonadotropic Hypogonadism Type 18
• Hypogonadotropic Hypogonadism Type 17
• Nephrotic Syndrome Type 8
• Severe Congenital Hypochromic Anemia with Ringed Sideroblasts
• ATP5A1-Related ATP Synthase Deficiency
• Postaxial Polydactyly Type A6
• Oculocutaneous Albinism Type 7
• Autosomal Recessive Monocyte and Dendritic Cell Deficiency
• Perrault Syndrome 3
• Epileptic Encephalopathy Type Lennox-Gastaut
• Amoxicillin
• Autosomal Dominant Cerebellar Ataxia - Deafness - Narcolepsy
• Craniosytosis Type 4
• Amoxapine
• X-Linked Deafness 6
• X-Linked Intellectual Disability Type Cantagrel
• Paroxysmal Nocturnal Hemoglobinuria Type 1
• Secondary Pulmonary Hypertension
• Contiguous ABCD1 DXS1357E Deletion Syndrome
• Amniotic Fluid Embolism
• High Myopia-Sensorineural Deafness Syndrome
• Amniotic Band
• Amnionitis
• Fetal Disorder
• Renal-Hepatic-Pancreatic Dysplasia 1
• Memory Impairment
• Ammonium Tetrathiomolybdate
• Ammonium Chloride
• Autosomal Dominant Hypocalcemia Type 1
• Autosomal Recessive Epidermolysis Bullosa Simplex
• Developmental Dysplasia of the Hip Type 2
• Isolated Brachycephaly
• Inhalation of Noxious Gases
• Familial Candidiasis Type 8
• Iodine-induced Hypothyroidism
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2T
• Autosomal Recessive Spastic Paraplegia Type 57
• Smith-McCort Dysplasia
• Meckel Syndrome
• Aminoglutethimide
• Autosomal Recessive Non-Syndromic Hydrocephalus
• Aminoaciduria
• Osteosclerotic Metaphyseal Dysplasia
• Metabolic Disorder of Amino Acids
• Bleeding Disorder Platelet Type 15
• Amipramizide
• Autosomal Recessive Dyskeratosis Congenita Type 5