×
This website uses cookies to ensure you get the best experience on our website.
Privacy
Okay
Any Age
years old
years
Any Age
Newborn
Toddler
Child
Teenager
Adult
Senior
Any Sex
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