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1001 to 2000 most common queries

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

Jackhammer Esophagus Primary Coenzyme Q10 Deficiency Type 8 Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain Proximal Monosomy 4q25 Autosomal Recessive Deafness 100 X-Linked Female-Restricted Facial Dysmorphism - Short Stature - Choanal Atresia - Intellectual Disability Progesterone-Receptor Negative Breast Cancer Primary Intrahepatic Lithiasis Mitochondrial Complex 1 Deficiency Nuclear Type 10 Ehlers-Danlos Syndrome Arthrochalasia Type 1 Bow Hunter's Stroke L-Cell Glucagon-Like Peptide Producing Tumor Juvenile-Onset Small-Fiber Polyneuropathy Microcephaly - Facial Abnormalities - Micromelia - Mental Retardation Cervical Neuroblastoma Female-Restricted X-Linked Syndromic Mental Retardation 99 Neurodevelopmental Disorder with Microcephaly - Epilepsy - Brain Atrophy Childhood-Onset Neurodegeneration with Ataxia - Dystonia - Gaze Palsy Apocrine Sweat Gland Neoplasm Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures Acute Macular Neuroretinopathy Hexahydrophthalic Anhydride Allergic Asthma Liver Fibrocystic Disease and Polydactyly Neurodevelopmental Disorder with Epilepsy and Hypoplasia of the Corpus Callosum Isolated HyperCKemia 16p12.2 Microdeletion 1,4-Phenylenediamine Allergic Contact Dermatitis Zebrafish Allergy ANKRD26-Related Thrombocytopenia Mitochondrial Complex 1 Deficiency Nuclear Type 24 Intraabdominal Hemangioma Mitochondrial Complex 1 Deficiency Nuclear Type 19 MYO5B-Related Progressive Familial Intrahepatic Cholestasis Childhood Thymoma Mitochondrial Complex 1 Deficiency Nuclear Type 27 ASAH1-Related Disorder Mosaic Trisomy 11 X-Linked Neurodevelopmental Disorder with Craniofacial Abnormalities Recurrent Idiopathic Neuroretinitis Sacral Nerve Root Cyst PLG-Related Hereditary Angioedema Mucopolysaccharidosis 9 AIP-Related Familial Isolated Pituitary Adenoma Nonsyndromic Hearing Loss and Deafness DFNX1 LAMA5-Related Multisystemic Syndrome Autosomal Recessive Anterior Segment Dysgenesis Myoclonic Epilepsy - Myopathy - Sensory Ataxia Autosomal Dominant Mental Retardation Type 40 Palladium Allergic Contact Dermatitis Mononeuritis of Upper Limb and Mononeuritis Multiplex Hypomyelinating Leukodystrophy Type 13 Horned Turban Snail Allergy Cardiomyopathy - Diabetes - Deafness Chromosome Y Pericentric Inversion 9q22.3 Microdeletion Mediastinal Mesenchymal Tumor 3-Methylglutaconic Aciduria Type 9 Tibial Hemimelia - Cleft Lip/Palate Neurodevelopmental Disorder with Epilepsy - Cataracts - Feeding Difficulties - Delayed Brain Myelination Spondyloepiphyseal Dysplasia Type Kondo-Fu Caribbean Parkinsonism Tetrachlorophthalic Anhydride Allergic Asthma Hyperpepsinogenemic 1 Duodenal Ulcer Autosomal Dominant Multiple Epiphyseal Dysplasia Cervical Endometrial Stromal Tumor Acro-Pectoro-Renal Field Defect Colobomata - Unilobar Lung - Heart Defect X-Linked Mental Retardation Type 107 Mixed Neuroendocrine-Nonneuroendocrine Neoplasm of the Pancreas Chondrodysplasia - Situs Inversus - Imperforate Anus - Polydactyly Chromosome 16p13.2 Deletion Syndrome Lissencephaly Type 8 Skeletal Dysplasia - T-Cell Immunodeficiency - Developmental Delay Dwarfism - Thin Bones - Multiple Fractures Specific Granule Deficiency 2 Generalized Lipodystrophy-Associated Progeroid Syndrome ARID1b-Related Disorder Hormone Producing Pituitary Cancer Autosomal Dominant Non-Syndromic Intellectual Disability 19 Congenital Aneurysms of the Great Vessels Flood Factor Deficiency Cerebellar Ataxia - Mental Retardation - Dysequlibrium Syndrome Diffuse Cavernous Hemangioma of the Rectum Epiphyseal Dysplasia of the Femoral Head - Myopia - Deafness Radius Aplasia with Cleft Lip/Palate Follicular Cholangitis and Pancreatitis Recurrent Hydatidiform Mole FLNB-Related Disorder Indian Plum Allergy Painful Legs and Moving Toes Syndrome Heritable Thoracic Aortic Disease Mucinous Bronchioloalveolar Adenocarcinoma Autosomal Dominant Nonsyndromic Deafness 34 CoQ-Responsive OXPHOS Deficiency Nonmucinous Bronchioloalveolar Adenocarcinoma Laugier-Hunziker Syndrome Autosomal Recessive Craniosynostosis Squamous Cell Carcinoma of the Corpus Uteri Mitochondrial Complex 1 Deficiency Nuclear Type 18 Recombinase Activating Gene 2 Deficiency Dwarfism - Mental Retardation - Eye Abnormality Mitochondrial Disease with Severe Hypotonia - Lactic Acidemia and Hyperammonemia Cerebello-Olivary Atrophy Apricot Allergy Tarsal Kink Syndrome UNC80 Deficiency Ichthyosis - Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin Preterm Premature Rupture of the Membranes 4-Tert-Butylphenol Allergic Contact Dermatitis X-Linked Syndromic Mental Retardation Type Houge Infertility due to Extratesticular Cause Mitochondrial Complex 1 Deficiency Nuclear Type 7 Multiple Paragangliomas Associated with Polycythemia Mitochondrial Complex 1 Deficiency Nuclear Type 25 Proteasome-Associated Autoinflammatory Syndrome 3 Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts Synostosis of Talus and Calcaneus - Short Stature Age-Related Macular Degeneration 2 Thumb Stiffness - Brachydactyly - Intellectual Disability Cone Rod Dystrophy Type 21 Colchicine Resistance Galloway-Mowat Syndrome Type 7 Palmoplantar Keratoderma of Sybert Multiple and Recurrent Inflammatory Fibroid Gastrointestinal Polyps Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 3 Combined Oxidative Phosphorylation Deficiency 35 Monosomy 6p Platelet-Activating Factor Acetylhydrolase Deficiency Recurrent Gastrointestinal Ulceration with Dysfunctional Platelets Rhizomelic Skeletal Dysplasia with Retinitis Pigmentosa CLPB Deficiency Band Keratopathy with Deafness HTRA1-Related Autosomal-Dominant Cerebral Small Vessel Disease Mesomycetozoea infection Melon Allergy ACSL4-Related Intellectual Disability PURA-Related Neurodevelopmental Disorder Male Infertility due to Spermatogenesis Disorder Mitochondrial Complex 5 Deficiency Nuclear Type 5 Dermal Unilateral Segmental Cavernous Angioma Female Breast Central Part Cancer Ocular Myopathy with Curare Sensitivity Midline Cleft of Lower Lip Duodenal Ulcer Due to Antral G-Cell Hyperfunction Autosomal-Recessive Pyridoxine-Refractory Sideroblastic Anemia 3 Indolent B-Cell Lymphoma Insulin-Dependent Diabetes Mellitus 8 Familial Ovarian Insufficiency DDX3X-Related Intellectual Disability Intellectual Developmental Disorder with Macrocephaly - Seizures - Speech Delay Mitochondrial Complex 1 Deficiency Nuclear Type 28 Cartilage-Hair Hypoplasia - Anauxetic Dysplasia Spectrum Disorder Opthalmic Icthyosis Dobrow Syndrome Ichthyosis - Split Hairs - Amino Aciduria Thrombocythemia with Distal Limb Defects Brachydactyly - Anonychia GARS-Associated Axonal Neuropathy Intellectual Disability - Hypotonia - Brachycephaly - Pyloric Stenosis - Cryptorchidism Unilateral Biphalangeal Duplication of the Thumb Kleefstra Syndrome 2 Asthma - Short Stature - Elevated IgA Cutis Laxa - Osteoporosis Lower Mesodermal Defects Sequence Intellectual Disability - Muscle Weakness - Short Stature - Facial Dysmorphism Facio-Skeletal-Genital Syndrome Rippberger Type Autosomal Recessive Spinocerebellar Ataxia with Axonal Neuropathy Type 3 Intellectual Developmental Disorder - Cardiac Defects - Dysmorphic Facies Lissencephaly 9 with Complex Brainstem Malformation Autosomal Dominant Spastic Paraplegia Type 80 Hypomyelinating Leukodystrophy Type 18 WAC-Related Intellectual Disability Trisomy 18-Like Syndrome Dwarfism - Bluish Sclerae Panic Disorder 1 Intellectual Developmental Disorder with Speech Delay - Dysmorphic Facies - T-Cell Abnormalities Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin Fetal Akinesia Deformation Sequence 4 Synostosis Perioral Myoclonia with Absences Autoimmune Atrophic Gastritis Talaromycosis Congenital Erosive and Vesicular Dermatosis LRP5-Related Primary Osteoporosis Short Limbs - Subluxed Knees - Cleft Palate Childhood Ovarian Cancer Microcephaly - Growth Deficiency - Seizures - Brain Malformation Mitochondrial Complex 1 Deficiency Nuclear Type 22 Multifocal Dystonia Age-Related Macular Degeneration 4 Parameningeal Embryonal Rhabdomyosarcoma Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 due to DGAT2 Mutation Pfeiffer Tietze Welte Syndrome MBD25-Related Intellectual Disability Short Limbs - Abnormal Face - Congenital Heart Disease PHIP-Related Disorder Familial Band Heterotopia Dermal Tumor Autosomal Recessive Nonsyndromic Deafness 108 Autosomal Dominant Nonsyndromic Deafness 71 Disorder of Intracellular Cobalamin Metabolism DCX-Related Disorders Neurological Consequences of Cytomegalovirus Infection NKX2-1-Related Disorders De Novo Thrombotic Microangiopathy after Kidney Transplantation Immune-Mediated Encephalomyelitis Syndromic Intrahepatic Biliary Atresia Epidermolysis Bullosa with Diaphragmatic Hernia Biliary Tract Neuroma Mental and Growth Retardation with Amblyopia Childhood Salivary Gland Cancer Deafness - Goiter - Stippled Epiphyses Pineal Parenchymal Tumor of Intermediate Differentiation Kyphoscoliosis - Lateral Tongue Atrophy - Hereditary Spastic Paraplegia Goat Milk Allergy Adult Progressive Spinal Muscular Atrophy Aran Duchenne Type Orgasm-Induced Seizures Salivary Gland-Type Cancer of the Breast Adams-Oliver Syndrome Type 6 Adams-Oliver Syndrome Type 1 Hypomyelinating Leukodystrophy Seckel Syndrome Type 1 Seckel Syndrome Type 10 Seckel Syndrome Type 6 Seckel Syndrome Type 9 Tamoxifene Resistance Oropharyngeal Anthrax Tympanic Membrane Disease Subcutaneous Mycosis Rete Ovarii Adenocarcinoma Chromium Allergic Contact Dermatitis Epiphora Due to Insufficient Drainage Malignant Giant Cell Tumor of Soft Parts Beach Ear Leukodystrophy and Acquired Microcephaly with or Without Dystonia Glioblastoma Neural Subtype Transvestism Cluttering Allopurinol Toxicity Congenital Autoimmune Diabetes Mellitus Orofacial Cleft PAFAH1B1-Associated Lissencephaly and Subcortical Band Heterotopia Peripapillary Staphyloma DICER1-Related Disorders Mitochondrial Complex 1 Deficiency Mitochondrial Type 1 PIK3CA-Related Overgrowth Spectrum Mitochondrial Complex 1 Deficiency Nuclear Type 31 Developmental Delay and Seizures with or Without Movement Abnormalities Orofaciodigital Syndrome Type 18 Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies Voriconazole Toxicity Lethal Hydranencephaly - Diaphragmatic Hernia Syndrome Noninsulin-Dependent Diabetes Mellitus 4 Segmental Outgrowth - Lipomatosis - Arteriovenous Malformation - Epidermal Nevus Malignant Neoplasm of Long Bones of Lower Limb Presbycusis 2 15q13.3 Microduplication Syndrome Fanconi-Like Syndrome Micturation-Induced Seizures Corneal Neuropathic Disease Jervell-Lange-Nielsen Syndrome Type 1 Sweat Gland Disease Misshapen Toe Formaldehyde Allergic Contact Dermatitis Lung Large Cell Carcinoma Glucoglycinuria Mucoepidermoid Lacrimal Gland Carcinoma Paratesticular Lipoma Tubular Adenocarcinoma Mucoepidermoid Breast Carcinoma Adult Dermatomyositis Neuroendocrine Prostate Neoplasm Congenital Amputation Trichoscyphodysplasia Solid Adenocarcinoma with Mucin Production Uterine Carcinosarcoma Keshan Disease Clear Cell Cystadenofibroma Clear Cell Squamous Cell Skin Carcinoma Pulmonary Artery Choriocarcinoma Uterine Corpus Endometrial Stromal Sarcoma Biliary Papillomatosis Anal Margin Carcinoma Signet Ring Cell Adenocarcinoma Proliferative Verrucous Leukoplakia Chromophobe Renal Cell Carcinoma Classic Variant Myxoid Ovarian Liposarcoma Reactive Angioendotheliomatosis Tyrosinosis Fibrocystic Breast Change Proliferative Type Urothelial Ureter Papilloma Gastrointestinal Lymphoma Malignant Anal Melanoma Metaplastic Breast Carcinoma Adult Liposarcoma Vascular Hemostatic Disease Squamous Cell Tonsil Carcinoma Combined Exocrine Pancreatic Insufficiency Thymus Basaloid Carcinoma Kosaki Overgrowth Syndrome Anti-Basement Membrane Glomerulonephritis Chronic Toxic Polyneuropathy Aspirin Allergy Endocardium Cancer Urachal Cancer Pediatric Mesenchymal Chondrosarcoma Breast Adenomyoepithelioma Cowper Gland Carcinoma Ocular Hypotension Prostate Leiomyoma Sarcomatoid Transitional Cell Carcinoma Flinders Island Spotted Fever Transient Retinal Arterial Occlusion Acetophenetidin Sensitivity Multiple Non Ossifying Fibromatosis Inverted Ureter Papilloma Ureteric Orifice Cancer Nipple Duct Carcinoma Pineal Region Germinoma Benign Anal Neoplasm Central Congenital Hypothyroidism Asbestos-Related Lung Carcinoma Oculomotor Nerve Tumor Benign Papillary Transitional Cell Urinary Tract Neoplasm Monckeberg Arteriosclerosis Urothelial Renal Pelvis Papilloma Vaginal Adenosarcoma Clear Cell Bile Duct Adenocarcinoma Cardiac Rupture Neurotrophic Keratoconjunctivitis Antidepressant Type Abuse Pleural Neurilemmoma Female Breast Lower-Inner Quadrant Cancer Myositis Fibrosa Botryoid Vaginal Rhabdomyosarcoma Inhibited Male Orgasm Sclerosing Breast Papilloma Adenoid Cystic Cervical Carcinoma Pubic Bone Dysplasia Villoglandular Endometrial Endometrioid Adenocarcinoma Tryptophanuria with Dwarfism Quinidine Allergy Ovarian Endometrioid Cancer Congenital Baculum Absence Atrophic Flaccid Tympanic Membrane Endocardial Fibroelastosis and Coarctation of Abdominal Aorta Retroperitoneal Neuroblastoma Intestinal Polyposis with Multiple Exostoses Histiocytic and Dendritic Cell Cancer Familial Macrocytosis Intraductal Papilloma Childhood Central Nervous System Immature Teratoma Chronic Lacrimal Passage Inflammation Mediastinal Leiomyoma Ovarian Angiosarcoma Lymphoepithelioma-Like Carcinoma Gastric Hemangioma Distal Chromosome 11p13 Deletion Syndrome Bilateral Medial Tibial Torsion Childhood Botryoid-Type Embryonal Vulvar Rhabdomyosarcoma Signet Ring Cell Bile Duct Carcinoma Colobomatous Macrophthalmia with Microcornea Light Fixation Seizure Syndrome Perivascular Epithelioid Cell Tumor Human Monocytic Ehrlichiosis Pauciarticular Juvenile Idiopathic Arthritis Malignant Mediastinal Neurogenic Neoplasm Familial Synovial Chondromatosis with Dwarfism Adult Brain Ependymoma Laryngeal Adductor Paralysis Epithelioid Type Angiomyolipoma Isolated Microphthalmia with Corectopia Large Cell Neuroendocrine Lung Carcinoma Open Angle Glaucoma Residual Stage Demyelinating Polyneuropathy Benign Eyelid Neoplasm Inflamed Seborrheic Keratosis Osteoporotic Fracture Segmental Spinal Muscular Atrophy Inverted Follicular Vulvar Keratosis Neuroendocrine Carcinoma Progressive Lymphoid System Deterioration Jejunal Somatostatinoma Hyperphosphatemia - Polyuria - Seizures Alpha-Thalassemia - Abnormal Morphogenesis Giant Cell Bone Sarcoma Mirror Agnosia Primary Open-Angle Glaucoma Type 1O Benign Shuddering Attacks Bier Spots Isolated Trihydroxycholestanoyl-Coa-Oxidase Deficiency Primary Open-Angle Glaucoma Type 1H Isolated Megalopapilla Duodenal Adenocarcinoma Nasal Cavity Inverting Papilloma Acute Allergic Sanguinous Otitis Media Lumbosacral Spina Bifida Aperta Congenital Craniosynostosis - Maternal Hyperthyroiditis Luteoma Mitochondrial Complex 1 Deficiency Nuclear Type 4 Extrahepatic Bile Duct Adenoma Congenital Vertebral-Cardiac-Renal Anomalies Syndrome Cellular Myxoid Liposarcoma Tamoxifen-Related Endometrial Lesion Nerve Plexus Neoplasm Akinetopsia Congenital Insensitivity to Pain with Severe Intellectual Disability Glucose-6-Phosphate Translocase Deficiency Adult Brainstem Gliosarcoma Lymphoma of the Small Intestine Short Stature - Amelogenesis Imperfecta - Skeletal Dysplasia with Scoliosis Prostate Embryonal Rhabdomyosarcoma Fallopian Tube Serous Papilloma Gallbladder Occlusion Lung Carcinoma in Situ Boylan Dew Greco Syndrome Pacinian Tumor Basal Cell Scrotal Carcinoma Epididymis Cancer Squamous Cell Vulvar Carcinoma Autotopagnosia Multilocular Encephalomalacia Glioblastoma Classical Subtype Oral Leukoedema Paralytic Lagophthalmos Esophageal Diverticulosis Phthisical Cornea Adult Epithelioid Sarcoma Vitreoretinal Dystrophy Tuberculous Oophoritis Mixed Gonadal Dysgenesis Childhood Kidney Angiomyolipoma Nuclear Senile Cataract Breast Hemangioma Anal Sarcoma Ileal Neuroendocrine Tumor Prediabetes Syndrome Liver Fibroma Pediatric Angiosarcoma Benign Breast Adenomyoepithelioma Drachtman Weinblatt Sitarz Syndrome Congenital Mydriasis Internal Auditory Canal Lipoma Neuroendocrine Esophageal Neoplasm Nephrogenic Adenofibroma Trichostrongyloidiasis Lip Carcinoma in Situ Serous Pancreatic Cystadenoma Sphenoorbital Meningioma Hypotrichosis - Progressive Patterned Scalp - Wiry Hair - Onycholysis - Cleft Lip/Palate Absence of Nasal Bones Mixed Malaria Carcinoid Neuroendocrine Small Intestine Tumor Clear Cell Ovarian Carcinoma Cystadenocarcinoma Tricho-Odonto-Onycho-Dermal Syndrome Transitional Papillary Carcinoma Brain Angioma Mixed Cerebral Palsy Hereditary Wilms' Tumor Angiomyomatous Hamartoma Enamel Hypoplasia - Cataract - Hydrocephaly Intellectual Developmental Disorder with Gastrointestinal Difficulties and High Pain Threshold Crab Allergy Female Breast Cancer Posttransplant Acute Limbic Encephalitis Mitochondrial DNA Depletion Syndrome 12A Pericoronitis Serous Surface Papilloma Medial Medullary Syndrome Hair Follicle Neoplasm Main Bronchus Cancer Non-Melanoma Skin Cancer in Childhood Faciothoracogenital Syndrome Intracanalicular Breast Fibroadenoma Childhood Testicular Choriocarcinoma Yao Syndrome Colon Leiomyoma Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids Adult Cerebellar Neoplasm X-Linked Vesicoureteral Reflux Optic Atrophy - Spastic Paraplegia Childhood Extraosseous Osteosarcoma Infundibulocystic Basal Cell Carcinoma Ovarian Seromucinous Carcinoma Cardiofacial Syndrome - Short Limbs Childhood Myocerebrohepatopathy Spectrum 5-Fluorouracil Poisoning Sarcomatous Intrahepatic Cholangiocarcinoma Thymus Lymphoma Mucoepidermoid Thyroid Carcinoma Carbapenem Allergy Phenytoin Allergy Urinary Bladder Atony Congenital Moderate Neural Deafness Benign Gastrointestinal System Neoplasm Familial Lipochrome Histiocytosis Ectopic Ethmoid Sinus Meningioma Pancreatic Cystadenoma Cervical Endometriosis Aztreonam Allergy Adrenal Gland Ganglioneuroblastoma Mastocytic Enterocolitis Nodular Basal Cell Carcinoma Vallecula Cancer Resistance to Vitamin K Antagonists Subcutaneous Panniculitis-Like T-Cell Lymphoma Childhood Brain Meningioma X-Linked Macular Dystrophy Small Intestine Hemangiomas Myotonic Cataract Cervicothoracic Spina Bifida Aperta Cutis Verticis Gyrata - Mental Deficiency Mucinous Colon Adenocarcinoma Tibial Adamantinoma Hereditary Cerebral Amyloid Angiopathy Polycythemia Due to Hypoxia Primary Eye Hypotony Renal Pelvis Adenocarcinoma Chromosome 18 Pericentric Inversion Adenosquamous Gastric Carcinoma Leg Dermatosis Supraglottic Neoplasm Childhood Central Nervous System Mature Teratoma Hereditary Bilateral Parotidomegaly Localized Chondrosarcoma Verrucous Papilloma Larynx Carcinoma in Situ Acneiform Dermatitis Chronic Uterine Subinvolution Absence of Peroneus Tertius Muscle Adenoid Cystic Prostate Carcinoma Atlantic Salmon Allergy Melanoma-Associated Retinopathy Infectious Myocarditis Spontaneous Tension Pneumothorax Exudative Glomerulonephritis Hypothalamic Neoplasm Epithelioid Cell Melanoma Childhood Rectal Cancer Malignant Granular Cell Myoblastoma Spitzoid Melanoma Non-Invasive Papillary Urothelial Bladder Neoplasm Benign Cerebrovascular Neoplasm Squamous Cell Skin Papilloma Tufted Hair Folliculitis Benign Bone Neoplasm Congenital Cardiovascular Shunt Pulmonary Bullae Causing Pneumothorax Rhabdoid Kidney Tumor Conjunctival Degeneration Infiltrating Angiolipoma Middle Ear Adenocarcinoma Pineal Dysgerminoma Central Cervical Cord Syndrome Great Toe Monophalangy Second Metatarsal-Metacarpal Syndrome 16p11.2 Deletion Syndrome Active Cochlear Meniere's Disease African Tick-Bite Fever Global Developmental Delay - Progressive Ataxia - Elevated Glutamine Venous Tributary Retinal Occlusion Proliferative Glomerulonephritis Amyloid Tumor Papillary Adenocarcinoma Age-Related Macular Degeneration 15 Adult Central Nervous System Primitive Neuroectodermal Neoplasm Benign Dermal Neurilemmoma Familial Nasal Polyposis Childhood Esophageal Cancer Subglottic Angioma Female Breast Nipple and Areola Cancer Multifocal Choroiditis Estrogen Receptor Positive Breast Cancer Atypical Polypoid Uterine Corpus Adenomyoma Familial Dyskeratotic Comedones Cervix Small Cell Carcinoma Uterine Corpus Bizarre Leiomyoma Keratoconus and Congenital Hip Dysplasia Juxtacortical Chondroma Breast Lymphoma Bile Duct Adenocarcinoma Cefotaxime Allergy Central Nervous System Osteosarcoma Secondary Lacrimal Atrophy Carotid Body Cancer Occult Large Cell Lung Carcinoma Nodding Syndrome Genetic Reflex Epilepsy Corpus Callosum Dysgenesis - Cleft - Spasm Integrated Human Herpesvirus 6 Ataxia with Fasciculations Spinal Bulbar Motor Neuropathy Snijders Blok-Campeau Syndrome Severe Influenza Epithelioid Bone Hemangioma DYRK1A-Related Intellectual Disability Variation in Skin/Hair/Eye Pigmentation 7 Chromosome 14q Duplication Senile Reticular Retinal Degeneration Split Hand-Split Foot with Hypodontia GLB1-Related Disorders Mucinous Stomach Adenocarcinoma Centrofacial Neurodysraphic Lentiginosis Mosaic Trisomy 3 Chromosome Xp Deletion Ossifying Fibromyxoid Tumor Keratoconus 2 FGFR-Related Craniosynostosis Syndromes Congenital Deafness and Familial Myoclonic Epilepsy Hereditary Essential Tremor 3 Mediastinal Sarcoma Pentasomy X Rubinstein Taybi Like Syndrome Retinal Lymphoma Solitary Chest Wall Plasmacytoma Chromosome 18q Duplication Photoallergic Dermatitis Extracranial Neuroblastoma Tomato Allergy Suprasellar Meningioma Heck Disease Ischemic Optic Neuropathy Clostridium Septicum Infection Progressive Locomotor Ataxia Impulse Control Disorder Familial Atrophia Maculosa Varioliformis Cutis Fallopian Tube Leiomyoma Childhood Nasal Cavity Carcinoma Granular Cell Neurohypophyseal Tumor Columnar Cell Variant Papillary Carcinoma Central Centrifugal Cicatricial Alopecia Anosognosia Central Nervous System Lipoma Conus Medullaris Neoplasm Pleuropneumonia Inflammatory and Toxic Neuropathy Signet Ring Cell Pancreatic Adenocarcinoma Benign Struma Ovarii Anal Carcinoma in Situ Kyphoscoliotic Heart Disease Serous Peritoneal Adenocarcinoma Eosinophilic Cryptitis Hereditary Vascular Retinopathy Familial Lichen Planus Diffuse Secondary Choroid Atrophy Multiple Mucosal Neuroma Leptomeningeal Sarcoma Mucinous Cystadenocarcinoma Cyclotropia Fordyce Angiokeratoma Necrotic Uveal Melanoma Multicentric Papillary Thyroid Carcinoma Hyperthyroxinemia Alveolar Orbit Rhabdomyosarcoma Extraskeletal Chondroma Hyperproglucagonemia Stroma-Dominant and Stroma-Poor Composite Ganglioneuroblastoma Congenital Nystagmus Cervical Adenocarcinoma Ovarian Yolk Sac Tumor Glandular Pattern Disaccharide Intolerance Macrodactyly of the Fingers Capillary Breast Hemangioma Invasive Transitional Cell Bladder Carcinoma Transitional Cell Ovarian Carcinoma Small Cell Thymus Carcinoma Maxillary Sinus Cancer Adult Acne Mucoepidermoid Bronchial Carcinoma Tracheal Sarcoma Glomangiomyoma Scirrhous Adenocarcinoma Bartholin's Gland Carcinoma Vulvar Sebaceous Carcinoma Breast Carcinoma in Situ Non-Squamous Non-Small Cell Lung Carcinoma Verrucous Carcinoma Spindle Cell Vaginal Epithelioma Adult Malignant Hemangiopericytoma Stomach Diverticulosis Glossopharyngeal Nerve Paralysis Trigeminal Nerve Neoplasm Orbital Leiomyoma Myelolymphatic Insufficiency Medullary Breast Carcinoma Multiple Syringomas Cervical Keratinizing Squamous Cell Carcinoma Bone Chondrosarcoma Myxosarcoma Bile Reflux Malignant Parametrium Neoplasm Parathyroid Gland Disease Childhood Brainstem Astrocytoma Choroid Epithelioid Cell Melanoma Metatarsus Adductus Central Nervous System Hemangioma Apocrine Breast Carcinoma Epithelioid Cell Ciliary Body Melanoma Clostridium Sordellii Infection Familial Idiopathic Priapism Non-Gestational Ovarian Choriocarcinoma Acute Diffuse Nephritis Multiple Spinal Canal and Spinal Cord Meningioma Testicular Yolk Sac Tumor Endodermal Sinus Pattern Intestinal Carcinoma in Situ Gonococcal Seminal Vesiculitis Mixed Epithelial Ovarian Tumor Chronic Intestinal Failure Cutaneous Bullous Amyloidosis Seminal Vesicle Tumor Cerebral Hemisphere Lipoma Oncocytic Breast Carcinoma Chronic Follicular Conjunctivitis Adrenal Rest Tumor Serous Cystic Pancreatic Neoplasm Pilarowski-Bjornsson Syndrome Mullerian Vaginal Papilloma Thyrotoxic Exophthalmos Aortic Dissection and Lentiginosis Syndrome Malignant Granular Cell Gastric Tumor Metachronous Wilms' Tumor Childhood Pilocytic Astrocytoma Laryngeal Neuroendocrine Tumor Malignant Melanocytic Peripheral Nerve Sheath Tumor of Mediastinum Chronic NK-Cell Lymphocytosis Testicular Brenner Tumor Necrotizing Gastritis Posterior Foramen Magnum Meningioma Childhood Parosteal Osteogenic Sarcoma Epithelial Predominant Wilms' Tumor Breast Myoepitheliosis Renal and Mullerian Duct Hypoplasia Monophasic Testicular Choriocarcinoma Amelia and Terminal Transverse Hemimelia Secondary Erythromelalgia Functioning Pancreatic Endocrine Tumor Neuroendocrine Rectal Neoplasm Lymphangiomatosis Symmastia Pancreatic Gastrinoma Barrett's Adenocarcinoma Mesenchymal Chondrosarcoma Basaloid Squamous Cell Cervical Carcinoma Villous Vaginal Adenoma Mental Retardation FRA12A Type Borst-Jadassohn Intraepidermal Carcinoma Neural Deafness with Atypical Atopic Dermatitis Gallbladder Pleomorphic Giant Cell Adenocarcinoma Persistent Genital Arousal Disorder Mixed Squamous Cell Penile Carcinoma Clear Cell Adenoma Bestiality Cervical Vertebral Dysplasia Pancreatic Foamy Gland Adenocarcinoma Parathyroid Oncocytic Adenoma Childhood Malignant Mesenchymoma Female Urethral Cancer Papillary Follicular Thyroid Adenocarcinoma Smooth Muscle Tumor Neonatal Urinary Tract Infection Adenoid Cystic Breast Carcinoma Raindrop Hypopigmentation Gonadal Stromal Sex Cord Tumor Rhabdomyomatous Mesenchymal Hamartoma Adult Teratoma Protein Z Deficiency Pyloric Atresia Uterine Corpus Adenofibroma Facial Hypertrichosis Childhood Penile Cancer Sclerosing Breast Adenosis Wolffian Duct Adenoma Suppurative Lymphadenitis Mixed Mucinous and Nonmucinous Bronchioloalveolar Adenocarcinoma Kidney Atheroembolism Autonomic Nervous System Neoplasm Verrucous Supraglottic Carcinoma Prosthetic Joint Infection Myocardial Stunning Ischemic Fasciitis Cavitary Optic Disc Anomalies Disseminated Eosinophilic Collagen Disease Solid Pattern Testicular Yolk Sac Tumor Chromosome 10q Deletion Tuberculous Empyema Sternal Lymphoma Congenital Panfollicular Nevus Neurovisceral Storage Disease with Curvilinear Bodies Adenosquamous Colon Carcinoma Ovarian Endodermal Sinus Tumor Papillary Adenofibroma Signet Ring Basal Cell Carcinoma Rokitansky-Aschoff Sinuses of the Gallbladder Gallbladder Squamous Cell Carcinoma Gallbladder Signet Ring Cell Adenocarcinoma Adult Type Testicular Granulosa Cell Tumor Anal Colloid Adenocarcinoma Extra-Adrenal Pheochromocytoma Multiple Skull Base Meningioma Hemidystonia Undritz Anomaly Glycogen-Rich Clear Cell Breast Carcinoma Intravascular Fasciitis Endocervicitis Postcricoid Region Cancer Childhood Choroid Plexus Cancer Birbeck Granule Deficiency Spindle Cell Iris Melanoma Posterior Lens Dislocation Childhood Cerebellar Neoplasm Optic Nerve Astrocytoma Malignant Epithelioid Hemangioendothelioma Adenoid Basal Cell Carcinoma Mixed Bladder Adenocarcinoma Squamous Cell Endometrial Carcinoma MEND Syndrome Esophageal Neurofibroma Central Pterygium Rete Testis Adenocarcinoma Ureteral Lymphoma Uterine Corpus Epithelioid Leiomyosarcoma Familial Dwarfism with Muscle Spasms Extrahepatic Biliary Papillomatosis Diaphragma Sellae Meningioma Escher Hirt Syndrome Diabetic Encephalopathy Lacrimal Punctum Eversion Childhood Small Cell Lung Carcinoma Plexiform Schwannoma Spermatic Cord Lipoma Anal Adenocarcinoma Uterine Corpus Adenomyoma Extracardiac Rhabdomyoma Childhood Endodermal Sinus Tumor Petit Fryns Syndrome Intracranial Embryonal Tumor Cervical Mullerian Papilloma Spindle Cell Rhabdomyosarcoma Tibial Neuropathy Uterine Corpus Lipoleiomyoma Extraventricular Neurocytoma Cervical Adenoma Malignum Vulvar Leiomyosarcoma Endothrix Pineal Gland Astrocytoma Mandibulofacial Dysostosis with Mental Retardation Clear Cell Vulvar Hidradenocarcinoma Angular Blepharoconjunctivitis Lateral Eye Displacement Chronic Hiccups Adult Pineal Parenchymal Tumor Common Bile Duct Neoplasm Cutler Bass Romshe Syndrome Cerebral Hypoxia Ametropic Amblyopia Hereditary Vertical Nystagmus Syphilitic Encephalitis Squamous Cell Breast Carcinoma Large Cell Keratinizing Variant Sebaceous Gland Neoplasm Amelogenesis Imperfecta Type 1J Amelogenesis Imperfecta Type 2A6 Amelogenesis Imperfecta Type 1F Heart Fibrosarcoma Gastrojejunal Ulcer Benign Peripheral Nervous System Neoplasm Mixed Endometrial Stromal and Smooth Muscle Tumor Aryepiglottic Fold Cancer Ceftazidime Allergy Infant Cerebrocortical Degeneration Malignant Leptomeningeal Tumor Grand Kaine Fulling Syndrome Heel Exostoses Early Congenital Syphilis Mixed Astrocytoma-Ependymoma-Oligodendroglioma Cloacogenic Rectal Carcinoma Clear Cell Ovarian Cystadenocarcinoma Optic Atrophy with Negative Electroretinograms Adult Central Nervous System Mixed Germ Cell Tumor Cellular Neurofibroma Alien Hand Syndrome Petroclival Meningioma Esophageal Leiomyosarcoma Adenoid Cystic Bartholin's Gland Carcinoma Mediastinal Neurilemmoma Dendritic Cell Thymoma Lopes-Maciel-Rodan Syndrome Dupuytren Subungual Exostosis Congenital Emphysema with Deafness, Penoscrotal Web and Mental Retardation Verrucous Vulvar Carcinoma Anal Lymphoma Kidney Hypertrophy Myoepithelial Breast Neoplasm Flat Retinoschisis Infiltrating Urothelial Bladder Carcinoma Microcystic Variant Brain Glioma Pediatric Lymphoma Cervical Adenosarcoma Viral Gastritis Splenic Sequestration Chronic Pericardial Effusion Benign Thoracic Neoplasm Steroid Lipomatosis Acquired Hemangioma Congenital Sulfhemoglobinemia Biphasic Synovial Sarcoma Ovarian Leiomyosarcoma Sphenocavernous Meningioma Central Nervous System Endodermal Sinus Tumor Breast Lipoma Seminal Vesicle Cystadenoma Central Nervous System Rhabdomyosarcoma Cephalosporin Allergy Sclerosing Cholangitis with Pancreatitis and Sicca Complex Pancreatic Delta Cell Neoplasm Chronic Erythremia Brain Ischemia Glutathione Peroxidase Deficiency Fallopian Tube Transitional Cell Carcinoma Pineal Region Meningioma Myxoid Uterine Corpus Leiomyoma Urachal Bladder Adenocarcinoma Kidney Osteogenic Sarcoma Adult Malignant Mesenchymoma Chronic Seminal Vesicle Gonorrhea Small Cell Neuroendocrine Urinary Bladder Carcinoma Conjunctival Intraepithelial Neoplasm Childhood Optic Tract Astrocytoma Mechanical Lagophthalmos Adult Choroid Plexus Tumor Cavernous Lymphangioma Chronic Erosive Gastritis Bladder Lateral Wall Cancer Inhibited Female Orgasm Pancreatic Sarcoma Mixed Astrocytoma-Ependymoma Onychocytic Matricoma Mixed Cell Choroid Melanoma Infiltrating Urothelial Bladder Carcinoma Clear Cell Variant Traumatic Glaucoma Adenosquamous Prostate Carcinoma Venous Hemangioma Absent Breasts and Nipples Bilateral Hyperactive Labyrinth Mucoepidermoid Thymic Carcinoma Paralytic Poliomyelitis Extragonadal Seminoma Gray Zone Lymphoma Female Reproductive Endometrioid Cancer Cervical Spinal Canal and Spinal Cord Meningioma Lumbar Spinal Canal and Spinal Cord Meningioma Micronodular Basal Cell Carcinoma Transitional Cell Prostate Carcinoma Seckel-Like Syndrome Type Majoor-Krakauer Sternal Tumor Intratubular Embryonal Carcinoma Malignant Histiocytic Disease Brain Stem Astrocytoma Human Spumaretrovirus Infection Galactorrhoea-Hyperprolactinaemia Glomangiomatosis Cryptogenic Multifocal Ulcerous Stenosing Enteritis Mixed Ductal Endocrine Carcinoma Epstein-Barr Virus Hepatitis Sarcomatoid Transitional Cell Kidney Pelvis Carcinoma Squamous Cell Tracheal Carcinoma Gonococcal Spondylitis Anal Leiomyosarcoma Mixed Germ Cell Sex Cord Neoplasm Kummell's Disease Rheumatic Pulmonary Valve Disease Serous Ovarian Adenocarcinoma Spindle Cell Lipoma Oropouche Fever Radiation Induced Cancer Spindle Cell Choroid Melanoma Ranitidine Allergy Polycystic Bone Disease Pancreatic Ductal Adenocarcinoma Sacral Spinal Canal and Spinal Cord Meningioma Scimitar Anomaly - Multiple Cardiac Malformations - Craniofacial and Central Nervous System Abnormalities Pyometritis Idiopathic Uveal Effusion Syndrome Corticosteroid-Sensitive Aseptic Abscesses Mixed Type Rhabdomyosarcoma Embryonal Extrahepatic Bile Duct Rhabdomyosarcoma Blue Toe Syndrome Squamous Cell Cervical Carcinoma Autoimmune Peripheral Neuropathy Benzo[d]isothiazol-3-One Allergic Contact Dermatitis RRM2B-Related Mitochondrial DNA Depletion Syndrome Large Cell Ovarian Neuroendocrine Carcinoma Neurogenic Palpebral Tumor Sticky Platelet Syndrome Bile Duct Mucinous Adenocarcinoma Ovarian Mucinous Adenofibroma Asternia Nonsyndromic Holoprosencephaly Inflammatory Leiomyosarcoma Nutritional Optic Neuropathy