201 to 500 most common queries

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

• Renal Impairment
• 2019 Novel Coronavirus Infection
• Klinefelter's Syndrome with XY/XXY Mosaic
• Sensorineural Hearing Loss
• Mandibulofacial Dysostosis
• Familial Episodic Pain Syndrome
• Amyotrophic Lateral Sclerosis
• Jugular Venous Distention
• Head Injury
• fibular aplasia tibial campomelia oligosyndactyly syndrome
• distal hereditary motor neuropathy type 2
• Trichorhinophalangeal Syndrome
• Treacher-Collins Syndrome Type 1
• Congenital Symmetric Circumferential Skin Creases Type 2
• Distal Hereditary Motor Neuropathy Type 9
• Auto-Brewery Syndrome
• COVID-19
• Isolated Growth Hormone Deficiency Type 5
• Isolated Growth Hormone Deficiency
• Congenital Hypomyelinating Neuropathy Type 3
• Congenital Hypomyelinating Neuropathy Type 2
• Congenital Hypomyelinating Neuropathy Type 1
• Dominant Intermediate Charcot-Marie-Tooth Disease Type G
• Charcot-Marie-Tooth Disease Type 2M
• Familial Thyroid Dyshormonogenesis
• Galloway-Mowat Syndrome Type 5
• Galloway-Mowat Syndrome Type 4
• Galloway-Mowat Syndrome Type 3
• Galloway-Mowat Syndrome Type 1
• Unilateral Hypoactive Labyrinth
• Sotos Syndrome Type 3
• Sotos Syndrome Type 1
• Cerebro-Oculo-Facio-Skeletal Syndrome Type 3
• Lymphatic Malformation Type 7
• Lymphatic Malformation Type 5
• Lymphatic Malformation Type 6
• Ehlers-Danlos Syndrome Classic-Like Type 2
• Bethlem Myopathy Type 1
• Bethlem Myopathy Type 2
• Ehlers-Danlos Syndrome Periodontitis Type 2
• Ehlers-Danlos Syndrome Spondylodysplastic Type 1
• Spondylocostal Dysostosis Type 1
• Spondylocostal Dysostosis Type 6
• Spondylocostal Dysostosis Type 5
• Craniosynostosis Type 6
• Craniosynostosis Type 1
• Neurodevelopmental Disorder with Poor Language - Loss of Hand Skills
• Leukocyte Disorder
• Familial Hemorrhagic Diathesis due to Antithrombin
• Rainbow Trout Allergy
• Mitochondrial Complex 1 Deficiency Nuclear Type 13
• X-Linked Hereditary Sensory and Autonomic Neuropathy
• PLA2G6-Associated Neurodegeneration
• Frontonasal Dysplasia - Phocomelic Upper Limbs
• Susceptibility to Visceral Leishmaniasis 3
• Ostertagiasis
• Malignant Neoplasm of the Upper Lip
• Neutrophil Chemotactic Response Abnormal
• Burn Scar
• Hemizygous Lethal Muscular Dystrophy
• Motility-Related Diarrhea
• Lower Extremity-Predominant Spinal Muscular Atrophy
• Bone Dysplasia Type Moore
• Early Infantile Epileptic Encephalopathy Type 72
• Monosomy 22q
• Collagenopathy Type 2 - Collagenopathy Type 11
• KCNQ2-Related Disorders
• Chromosomal Instability with Tissue-Specific Radiosensitivity
• Hemopoietic Proliferation
• Critical Limb Ischemia
• Precocious Epileptic Encephalopathy
• Susceptibility to Neuroblastoma 7
• Hypomyelinating Leukodystrophy Type 16
• Mosaic Trisomy 12
• Diaphragmatic Hernia - Upper Limb Defects
• Microdontia - Hypodontia - Short Stature
• Localized Hypertrophic Neuropathy
• Marfanoid Habitus - Inguinal Hernia - Advanced Bone Age
• Uncombable Hair Syndrome Type 2
• Selective Tooth Agenesis Type 7
• Fatal Infantile Encephalomyopathy
• Mitochondrial Complex 5 Deficiency Mitochondrial Type 1
• 46,XX Gonadal Dysgenesis with Short Stature - Recurrent Metabolic Acidosis
• Linear Hamartoma Syndrome
• Intellectual Developmental Disorder with Hypertelorism - Distinctive Facies
• Susceptibility to Opioid Dependence 1
• X-Linked Mental Retardation Type 102
• Neurodevelopmental Disorder with Hypotonia - Seizures - Absent Language
• SIX2-Related Frontonasal Dysplasia
• Abnormal Bone Structure
• Benign Reproductive Organ Neoplasm
• Syngnathia - Cleft Palate
• Cyanosis and Hepatic Disease
• TBC1D24-Related Disorders
• Developmental Coordination Disorder
• Hereditary Ataxia Type Schut-Book
• Age-Related Macular Degeneration Type 5
• Familial Hypertrophic Cardiomyopathy Type 15
• Language Delay - Attention Deficit-Hyperactivity Disorder/Cognitive Impairment - Cardiac Arrhythmia
• KAT6B-Related Disorders
• Limbic Encephalitis with Neurexin-3 Antibodies
• RRM2B-Related Mitochondrial Disease
• Susceptibility to Graves Disease 2
• Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia - Cortical Malformations
• Combined Oxidative Phosphorylation Defect Type 36
• Symphalangism - Short Stature - Accessory Testis
• Short Stature - Deafness - Neutrophil Dysfunction - Dysmorphism
• Idiopathic Generalized Epilepsy Type 3
• Corneal Dystrophy - Pigmentary Anomaly - Malabsorption
• Short Broad Great Toe - Macrocranium
• C9ORF72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
• Autosomal Recessive Non-Syndromic Deafness Type DFNB107
• Trisomy 21q
• Microcephaly - Facial Dysmorphism - Ocular Anomalies - Multiple Congenital Anomalies
• Ehlers-Danlos Syndrome Type Friedman-Harrod
• Pyoderma Gangrenosum - Acne - Suppurative Hidradenitis
• Cardiac-Type Muscular Dystrophy
• Non-Papillary Renal Cell Carcinoma
• Duane Syndrome Type 3
• Susceptibility to Spondyloarthropathy 3
• Ipp-Gelfand Syndrome
• Charcot-Marie-Tooth Disease Type Guadalajara
• Panic Disorder Type 2
• Neurodevelopmental Disorder with Progressive Microcephaly - Spasticity - Brain Anomalies
• Nephrotic Syndrome - Ocular Anomalies
• Myosinopathy
• Odonto-Onycho Dysplasia with Alopecia
• Arthrogryposis - Intrauterine Growth Retardation - Thoracic Dystrophy
• Stomatocytosis Type 2
• Monosomy 2p
• Diffuse Hyperinsulinism
• Vasculitis Syndromes of the Nervous System
• Mid-Dermal Elastolysis
• Age-Related Macular Degeneration Type 8
• Punctate Acrokeratoderma - Freckle-Like Pigmentation
• Polymicrogyria - Ehlers-Danlos Syndrome Type 4
• Muscular Dystrophy Type Barnes
• Benign Sensory System Neoplasm
• Cone-Rod Dystrophy - Hearing Loss
• Specific Language Impairment Type 4
• Malignancy Diagnosed during Pregnancy
• Linear Focal Elastosis
• Autosomal Dominant Radiation Sensitivity-Chromosome Instability Syndrome
• Piepkorn Dysplasia
• Sigmoid Disease
• Susceptibility to Spondyloarthropathy 2
• Otosclerosis Type 5
• Craniofacial Anomalies - Anterior Segment Dysgenesis
• Laryngeal Cleft
• Lethal Neonatal Autosomal Recessive Axonal Sensorimotor Polyneuropathy
• Acquired Angioedema with C1Inh Deficiency
• Microcephaly - Complex Motor and Sensory Axonal Neuropathy
• FBLN5-Related Cutis Laxa
• Vaginal Endometrial Stromal Neoplasm
• Non-Viral Serous Conjunctivitis
• Bartholin's Gland Disease
• Optic Atrophy Type 1 - Deafness
• Blepharo-Naso-Facial Syndrome Type Van Maldergem
• INSR-Related Severe Syndromic Insulin Resistance
• Amino Aciduria - Mental Deficiency - Dwarfism - Muscular Dystrophy - Osteoporosis - Acidosis
• TANGO2-Related Metabolic Encephalopathy and Arrhythmias
• Friedreich-Like Ataxia - Optic Atrophy - Sensorineural Deafness
• Cassavism
• Central Nervous System Hematopoietic Neoplasm
• CD79B Deficiency
• Flushing of Ears - Somnolence
• X-Linked Mental Retardation Type 105
• Grouped Pigmentation of the Retina
• BSCL2-Related Neurologic Disorders
• Ectopic Eruption of Teeth
• Syndromic Mental Retardation
• Male Infertility with Monogenic Teratozoospermia
• Cerebral Calcifications - Opalescent Teeth - Phosphaturia
• Prepapillary Vascular Loops
• Trisomy 22q
• Familial Partial Epilepsy
• Limb Ischemia
• Mitochondrial Complex 1 Deficiency Nuclear Type 14
• Ectrodactyly of the Lower Limbs - Congenital Heart Defect - Micrognathia
• WFS1-Related Disorders
• Hereditary Coagulation Disorder
• Small-Intestine Neuroendocrine Tumor
• Parenchymatous Neurosyphilis
• Age-Related Macular Degeneration Type 14
• Monogenic Diabetes
• Patent Blue V Allergy
• Childhood Electroclinical Syndrome
• Tetralogy of Fallot - Glaucoma
• Chloramine-T Respiratory Allergy
• Cefotiam Allergy
• Non-A-E Hepatitis
• Mitochondrial DNA Deletion Syndrome
• Reduction in Two-Point Discrimination
• Primitive Neuroectodermal Tumor of the Cervix Uteri
• Combat Neurosis
• Pre-Malignant Neoplasm
• Altered Metabolism of Coumarin
• Chondroitin-6-Sulfaturia - Defective Cellular Immunity - Nephrotic Syndrome
• Childhood Carcinoma of Unknown Primary Site
• Facial Dysmorphism - Hypertrichosis - Epilepsy - Mental Retardation - Developmental Delay - Gingival Overgrowth
• 16p12.1-p12.3 Triplication Syndrome
• Semmekrot-Haraldsson-Weemaes Syndrome
• KCNT1-Related Epilepsy
• Diethylthiourea Allergic Contact Dermatitis
• Retinal Dystrophy - Iris Coloboma - Congenital Cataract
• X-Linked Mental Retardation Type 61
• Multiple Impacted Teeth
• Commensal Bacterial Infectious Disease
• Laryngeal Atresia - Encephalocele - Limb Deformities
• Autosomal Dominant Mental Retardation Type 48
• Spermatogenic Failure Type 36
• Congenital Mumps
• Non-Secreting Chemodectoma
• Multiple Synostoses Syndrome Type 4
• Keratoconus Type 8
• TP63-Related Disorders
• Early Infantile Epileptic Encephalopathy Type 74
• Ankyloblepharon Filiforme Adnatum - Imperforate Anus
• KSHV Inflammatory Cytokine Syndrome
• Congenital Cataract - Severe Neonatal Hepatopathy - Global Developmental Delay
• X-Linked Mental Retardation Type 108
• Infantile Hypotonia with Psychomotor Retardation - Characteristic Facies Type 2
• Ring Corneal Ulcer
• Congenital T-Cell Immunodeficiency
• Intellectual Developmental Disorder with Short Stature - Facial Anomalies - Speech Defects
• Neurodevelopmental Disorder with Dysmorphic Facies - Distal Limb Anomalies
• Superficial Punctate Keratopathy Type Thygeson
• Wiedemann-Opitz Syndrome
• Malignant Buccal Mucosa Neoplasm
• Early-Onset Progressive Encephalopathy with Brain Edema - Leukoencephalopathy Type 2
• Extrinsic Cardiomyopathy
• Diaphragmatic Agenesis - Radial Aplasia - Omphalocele
• Gigantism - Advanced Bone Age - Hoarse Cry
• Familial Hypertrophic Cardiomyopathy Type 27
• Whitewater Arroyo Hemorrhagic Fever
• Age-Related Macular Degeneration Type 12
• Acute Poisoning by Drugs with Membrane-Stabilizing Effect
• Motor Neuron Disease with Dementia - Ophthalmoplegia
• Multiple Types of Congenital Heart Defects Type 3
• Immunodeficiency Type 60
• Serotonin-Producing Pancreatic Neuroendocrine Tumor
• Keratoconus Type 1
• Encephalocele - Anencephaly
• Neurodevelopmental Disorder with Cerebellar Atrophy - Seizures
• Hereditary Motor and Sensory Neuropathy - Retinitis Pigmentosa
• Fryns-Fabry-Remans Syndrome
• Non-Functioning Paraganglioma
• CD4 Deficiency
• Eye Movement Disorder
• Emilin-1-Related Connective Tissue Disorder
• Short Stature - Monodactylous Ectrodactyly - Cleft Palate
• Variation in Skin/Hair/Eye Pigmentation Type 1
• Pediatric Aortic Valve Stenosis
• Autosomal Recessive Spinocerebellar Ataxia Type 27
• Craniosynostosis - Arthrogryposis - Cleft Palate
• Autosomal Recessive Microcephaly with Chorioretinopathy Type 3
• Malignant Germ Cell Neoplasm of the Cervix Uteri
• Chronic Orthostatic Intolerance
• Intellectual Developmental Disorder with Dysmorphic Facies - Ptosis
• Childhood-Onset Progressive Contractures - Limb-Girdle Weakness - Muscle Dystrophy
• Gallbladder Disease Type 3
• Cavernous Transformation of the Portal Vein
• Painful Orbital and Systemic Neurofibromas - Marfanoid Habitus
• Trochleitis
• Symphalangism - Brachydactyly - Craniosynostosis
• Autosomal Recessive Mentale Retardation Type 58
• HaNDL Syndrome
• Hypoplastic Thumb - Müllerian Aplasia
• Timothy Grass Allergy
• D-Lactic Aciduria
• Distal Arthrogryposis Type 2B2
• GRIN1-Related Neurodevelopmental Disorder
• Visual Pathway Disorder
• Prelingual Non-Syndromic Genetic Deafness
• Autoimmune Disease of the Gastrointestinal Tract
• Sternal Malformation - Vascular Dysplasia
• Intermediate Charcot-Marie-Tooth Disease
• Familial Omphalocele Syndrome with Facial Dysmorphism
• Familial Juvenile Hyperuricemic Nephropathy
• MYBPC1-Related Autosomal Recessive Non-Lethal Arthrogryposis Multiplex Congenita Syndrome
• Bipolar 2 Disorder
• 4-Vinylcyclohexene Dioxide Respiratory Allergy
• 9q33.3-q34.11 Microdeletion Syndrome
• APOE p.Leu167del-Related Lipid Disorders
• Short Stature - Valvular Heart Disease
• Primary Oculocerebral Lymphoma
• Tubulinopathy
• MDA5 Deficiency
• Circumscribed Disseminated Keratosis Type Jadassohn-Lew
• Hereditary Neuropathy
• Israeli Tick Typhus
• Fetal Akinesia Deformation Sequence Type 3
• Skeletal-Extraskeletal Angiomatosis
• Autosomal Dominant Myopia - Midfacial Retrusion - Sensorineural Hearing Loss - Rhizomelic Dysplasia
• Core-Binding Factor Acute Myeloid Leukemia
• Congenital Diarrhea Type 10
• SOX2-Related Eye Disorders
• Metatarsus Varus Type 1
• Congenital Progressive Bone Marrow Failure - B-Cell Immunodeficiency - Skeletal Dysplasia Syndrome
• Mitochondrial Complex 1 Deficiency Nuclear Type 32