Sitemap | Symptoma

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