15401 to 15500 most common queries

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

• Stickler Syndrome Type 3
• Actinobacillus Infection
• Syndactyly, Type 4
• Non-Communicating Isolated Syringomyelia
• Corticotropin
• Thrombocytopenia 2
• Thrombophilia due to Activated-Protein C Resistance
• Hereditary Multiple Trichodiscomas
• Trichorhinophalangeal Syndrome Type 1 and 3
• Familial Hypertrophic Cardiomyopathy Typ 7
• Acroosteolysis
• Autosomal Dominant Congenital Nystagmus Type 4
• Renal Injury
• Ablepharon Macrostomia Syndrome
• Neuroectodermal Melanolysosomal Disease
• Diffuse Corticomeningeal Angiomatosis of Divry and Van Bogaert
• Anophthalmia or Microphthalmia - Esophageal Atresia Syndrome
• Arterial Tortuosity Syndrome
• Ataxia-Oculomotor Apraxia Syndrome
• Bardet-Biedl Syndrome Type 11
• Bardet-Biedl Syndrome 10
• Bardet-Biedl Syndrome Type 9
• Postural Defect
• Osteoarthritis of the Knee
• Microcephalic Osteodysplastic Primordial Dwarfism Types 1 and 3
• Lethal Bone Dysplasia, Holmgren Type
• Hereditary Arterial and Articular Multiple Calcification Syndrome
• Camptodactyly Syndrome Guadalajara Type 1
• Venous Thrombosis
• Familial Candidiasis Type 2
• Premature Centromere Division
• Autosomal Recessive Spinocerebellar Ataxia
• Griscelli Syndrome Type 1
• Long QT Syndrome 3
• Multiple Endocrine Neoplasia Type 1
• Inguinal Hernia
• Secondary Hypothyroidism
• Congenital Hereditary Facial Paralysis with Variable Hearing Loss
• Autosomal Dominant Spastic Paraplegia Type 10
• Generalized Epilepsy with Febrile Seizures plus Type 3
• Blepharophimosis - Intellectual Disability Syndrome Type Verloes
• Spinal Muscular Atrophy with Respiratory Distress Type 1
• Autosomal Recessive Primary Microcephaly 4
• Familial Febrile Convulsions 4
• Familial Focal Epilepsy with Variable Foci
• Chronic Hepatitis
• Nephronophthisis 3
• Familial Isolated Arrhythmogenic Right Ventricular Dysplasia
• Hereditary Motor and Sensory Neuropathy Type Okinawa
• Trichotillomania
• Immunodeficiency due to Defective Expression of HLA Class 1
• Autosomal Recessive Congenital Ichthyosis Type 5
• Dysidrosis
• Huntington Disease-Like 3
• Autosomal Dominant Spastic Paraplegia Type 12
• Stickler Syndrome Type 2
• Gonadal Dysgenesis
• Autosomal Recessive Deafness 44
• MORM Syndrome
• Familial Isolated Arrhythmogenic Right Ventricular Dysplasia 10
• Infantile Neuroaxonal Dystrophy 1
• Macular Coloboma - Cleft Palate - Hallux valgus Syndrome
• Craniofacial Dyssynostosis
• Estrogenic Agents
• Esophageal Diverticula 
• Presenile Dementia with Bone Cysts
• Kirghizian Dermatoosteolysis
• Rhizomelic Chondrodysplasia Punctata Type 2
• Dysmyelination with Jaundice
• Primary Dystonia Type DYT2
• Saethre-Chotzen Syndrome
• Ependymoma
• Acrocephalopolysyndactyly
• Encephalitis Lethargica
• Eisenmenger Syndrome
• Acquired Sideroblastic Anemia
• Primary Congenital Glaucoma 3A
• Acquired Factor XIII Deficiency
• Chronic Granulomatous Disease due to NCF2 Deficiency
• Acquired Disorder
• Congenital Bile Acid Synthesis Defect Type 2
• Naguib Syndrome
• Hypertelorism and Tetralogy of Fallot
• Congenital Generalized Hypertrichosis
• Antenatal Bartter Syndrome
• Hypercatabolic Hypoproteinemia
• Autosomal Recessive Channelopathy-Associated Insensitivity to Pain
• Nephronophthisis 1
• Sudden Hearing Loss
• Ketoadipicaciduria
• Deafness
• Quercus Poisoning
• Occupational Acne
• Lymphedema Hypoparathyroidism Syndrome
• Cystic Acne Vulgaris
• Autosomal Recessive Spastic Paraplegia Type 21
• Oto-spondylo-megaepiphyseal Dysplasia
• Papillary Cystadenoma
• Metaphyseal Acroscyphodysplasia
• Metaphyseal Chondrodysplasia Type Kaitila