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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
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
Odd Shapes of Teeth