15701 to 15800 most common queries

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

• Cataract - Congenital Heart Disease - Neural Tube Defect Syndrome
• Hermansky-Pudlak Syndrome
• Autosomal Dominant Mandibulofacial Dysostosis with Ptosis
• Craniosynostosis with Ocular Abnormalities and Hallucal Defects
• Peritoneal Disease
• Autosomal Dominant Congenital Nystagmus 3
• Spondyloepiphyseal Dysplasia Type Kimberley
• Autosomal Recessive Primary Microcephaly 6
• Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1F
• Juvenile Onset Primary Open-Angle Glaucoma 1
• Familial Progressive Cardiac Conduction Defect Type 2
• Familial Progressive Hyper- and Hypopigmentation
• Single Central Maxillary Incisor
• Congenital Autosomal Dominant Indifference to Pain
• Intracranial Abscess
• X-Linked Diffuse Leiomyomatosis-Alport Syndrome
• Prieto Syndrome
• X-Linked Congenital Nystagmus Type 1
• X-Linked Recessive Charcot-Marie-Tooth Disease Type 5
• Early Infantile Epileptic Encephalopathy Type 2
• Spastic Paraplegia Type 2
• Taurodontism Microdontia and Dens Invaginatus
• Atypical Facial Pain
• Hypocalcemic Vitamin D-Dependent Rickets Type 1B
• Retinitis Pigmentosa 11
• Neuronal Ceroid Lipofuscinosis 7
• Uterine Fibroid
• Oculomaxillofacial Dysostosis
• Toriello-Lacassie-Droste Syndrome
• Multiple Epiphyseal Dysplasia Type 1
• Enteropathy, Familial with Villous Edema and IgG2 Deficiency
• Increased Sweating
• CODAS Syndrome
• Autosomal Dominant Lateral Temporal Lobe Epilepsy
• Autosomal Recessive Mental Retardation 3
• Lattice Corneal Dystrophy Type 3A
• Congenital Corneal Opacities - Cornea Guttata - Corectopia
• Leber Congenital Amaurosis Type 9
• Familial Sick Sinus Syndrome
• Joubert Syndrome Type 3
• Susceptibility to Asperger Syndrome 1
• Autosomal Dominant Deafness 28
• Spinocerebellar Ataxia Type 20
• AICA-Ribosiduria
• Adult-Onset Hereditary Sensory and Autonomic Neuropathy with Anosmia
• Spondyloepimetaphyseal Dysplasia Type Matrilin-3
• Ehlers Danlos Syndrome Beasley Cohen Type
• Pelizaeus-Merzbacher-Like Disease Type 1
• Leukoencephalopathy - Arthritis - Colitis - Hypogammaglobulinema
• Congenital Muscular Dystrophy Type 1D
• Myopia 6
• Vitamin A Deficiency
• Familial Atrial Fibrillation 3
• Marfanoid Habitus with Situs Inversus
• Peripheral Cone Dystrophy
• Narcolepsy 3
• Autosomal Recessive Spastic Paraplegia Type 27
• Neuronal Ceroid Lipofuscinosis 9
• Autosomal Dominant Nonsyndromic Auditory Neuropathy
• Czech Metatarsal Dysplasia
• Hypotrichosis 7
• Loeys Dietz Syndrome Type 1
• Autosomal Recessive Spastic Paraplegia Type 26
• Pancreatic Heterotopia
• Griscelli Syndrome Type 3
• Schindler Disease, Type 1
• Familial Febrile Convulsions Type 6
• Familial Febrile Convulsions FEB5
• Myopia 7
• Myopia 8
• Myopia Typ 10
• Autosomal Dominant Charcot-Marie-Tooth Disease Type 2A2
• Nemaline Myopathy 6
• Autosomal Dominant Progressive External Ophthalmoplegia Type 2
• Nemaline Myopathy 1
• Autosomal Dominant Progressive External Ophthalmoplegia Type 3
• Spinocerebellar Ataxia Type 26
• Abdominal Muscle Strain
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2K
• MEDNIK Syndrome
• Multiple Epiphyseal Dysplasia - Severe Proximal Femoral Dysplasia
• Multiple Epiphyseal Dysplasia with Miniepiphyses
• Cataract 35
• Acromesomelic Chondrodysplasia with Genital Anomalies
• Generalized Epilepsy - Paroxysmal Dyskinesia Syndrome
• Myofibrillar Myopathy Type 4
• Classic Progressive Supranuclear Palsy Syndrome
• Congenital Merosin-Positive Muscular Dystrophy
• Thromboembolism
• Amyotrophic Lateral Sclerosis 17
• Autosomal Recessive Deafness 23
• Resistance to Clopidogrel
• Spastic Paraplegia - Optic Atrophy - Neuropathy Syndrome
• Familial Anomalous Origin of Right Pulmonary Artery
• Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 1
• Autosomal Recessive Spastic Paraplegia Type 30
• Autosomal Recessive Ichthyosis with Hypotrichosis ARCI11
• Congenital Malrotation of the Colon
• Epiphyseal Dysplasia Type Baumann
• Nonsyndromic Renal Hypodysplasia Type 1