1001 to 2000 most common queries

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

• Otosclerosis 2
• 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