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Mesenchymoma Alcohol-Induced Mental Disorder Synovial Neoplasm Duarte Variant Galactosemia Wolffian Duct Adenocarcinoma Nephrogenic Urinary Bladder Adenoma Rectal Leiomyoma Pelvic Varices Testicular Fibroma Malignant Renovascular Hypertension Prostate Stromal Sarcoma Brachmann-De Lange-Like Facial Changes with Microcephaly, Metatarsus Adductus, and Developmental Delay Sex Cord-Stromal Benign Neoplasm Neurodevelopmental Disorder with Severe Motor Impairment and Absent Language Pseudopapilledema Degenerative Eyelid Disease Ureter Squamous Cell Carcinoma Neuroaspergillosis Breast Hemangiopericytoma Indolent Myeloma Mediastinal Osteogenic Sarcoma Parasitic Eyelid Infestation Epithelial Predominant Pulmonary Blastoma Cystic Hypersecretory Breast Carcinoma Endometrial Small Cell Carcinoma Primary T-Cell Immunodeficiency Littre's Glands Carcinoma Ovarian Serous Cystadenocarcinoma Thymus Clear Cell Carcinoma Mucinous Ovarian Cystadenoma Age-Related Nuclear Cataract Clear Cell Ependymoma Testicular Polyembryoma Autosomal Dominant Pontine Microangiopathy with Leukoencephalopathy Spindle Cell Intraocular Melanoma Familial Calcification of Superior Transverse Scapular Ligament Coloboma Porencephaly Hydronephrosis Pediatric Cerebral Ependymoblastoma Gasserian Ganglion Meningioma Stromal Predominant Kidney Wilms' Tumor Episcleritis Periodica Fugax Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract Childhood Thyroid Cancer Dystrophinopathies Cholestasis with Gallstone, Ataxia, and Visual Disturbance Pituitary Infarct Abnormal Threshold of Rods Benzylpenicillin Allergy Imperforate Oropharynx-Costovertebral Anomalies Syndrome Papillary Clear Cell Bladder Adenocarcinoma Endometrial Mixed Adenocarcinoma Central Nervous System Germinoma Partial Retinal Artery Occlusion Cellular Congenital Mesoblastic Nephroma Multiple System Atrophy with Orthostatic Hypotension Ocular Hyperemia Geotrichosis Renal Artery Atheroma Intrapelvic Lymph Node Leukemic Reticuloendotheliosis Anterior Optic Tract Meningioma Corpus Callosum Lipoma Mixed Epithelial/mesenchymal Metaplastic Breast Carcinoma Endocrine Pancreas Disease Remitting Seronegative Symmetrical Synovitis with Pitting Edema Stalker Chitayat Syndrome Tristichiasis Cormier Rustin Munnich Syndrome Disseminated Sclerosis with Narcolepsy Presenile Kraepelin Type Dementia Upper Limb Mononeuritis Tonsillar Pillar Cancer Cervical Adenoid Basal Carcinoma Collagenous Gastritis Lateral Ventricle Meningioma Childhood Vagina Botryoid Rhabdomyosarcoma Equatorial Staphyloma Borderline Intellectual Functioning Mild Mental Retardation Childhood Ovarian Embryonal Carcinoma Bladder Tuberculosis Actinobacillosis Neonatal 6q24-Related Transient Diabetes Mellitus Pediatric Intraocular Retinoblastoma Lung Adenoid Cystic Carcinoma Gastric Pylorus Carcinoma Abducens Nerve Neoplasm Rocuronium Allergy Eyelid Allergic Contact Dermatitis Familial Right Atrium Dilatation Anal Margin Squamous Cell Carcinoma Overnutrition Conjugated Hyperbilirubinemia Type 3 Gestational Ovarian Choriocarcinoma Pineal Region Choriocarcinoma Orofacial Granulomatosis Tuberculous Salpingitis 3-Methylglutaconic Aciduria Type 8 Double Inferior Vena Cava Substance-Induced Psychosis Acute Gonococcal Epididymo-Orchitis Necrotic Choroidal Melanoma Cerebral Creatine Deficiency Syndrome Giant Hemangioma Myeloid and Lymphoid Neoplasms with FGFR1 Abnormalities Complex Cortical Dysplasia with Other Brain Malformations Postsurgical Hypothyroidism HER2-Receptor Negative Breast Cancer Patternless Dermal Ridges Hypertaurinuric Cardiomyopathy Bone Marrow Monosomy 7 Gallbladder Melanoma Melanocytic Psammomatous Malignant Peripheral Nerve Sheath Tumor Diffuse Cystic Renal Dysplasia Complex Cortical Dysplasia with Other Brain Malformations Type 9 Letrozole Toxicity Colloid Adenoma Familial Candidiasis Type 9 Viral Esophagitis Prepuce Cancer Posterior Exchondrosis of the Pinna Tubulinopathy-Associated Dysgyria Triple-Negative Breast Cancer Neutrophil Actin Dysfunction Autosomal Dominant Nonsyndromic Deafness 73 Epiblepharon of Upper Lid Pilomatrix Carcinoma of the Skin Chromosome 7p Deletion Epiglottic Cancer Autoimmune Polyendocrine Syndrome Type 4 Gestational Diabetes Insipidus Auditory Agnosia Nested Variant of Urothelial Carcinoma Hyperzincemia with Functional Zinc Depletion Pulmonary Artery Leiomyosarcoma Nipple Neoplasm Sebaceous Carcinoma of the Breast Marginal Glioneuronal Heterotopia Sickle Cell Disease Associated with Another Hemoglobin Anomaly Familial Streblodactyly Extrapulmonary Tuberculosis Acid Anhydride Respiratory Allergy Follicular Basal Cell Carcinoma Type 2 Collagen Defect Papillary Transitional Cell Carcinoma of the Bladder Malignant Tumor of the Pyloric Antrum Synchronous Multifocal Osteogenic Sarcoma Craniosynostosis - Mental Retardation - Heart Defects Cochlear Nerve Deficiency Mondor Disease Stromal Corneal Pigmentation Extragonadal Mixed Germ Cell Tumor Eccrine Porocarcinoma Placental Choriocarcinoma Ovarian Clear Cell Adenocarcinoma Childhood Mediastinal Neurogenic Tumor Mitochondrial Complex 1 Deficiency Nuclear Type 15 Pulmonary Adenoma Paranasal Sinus Lymphoma Vulvar Trichoepithelioma Squamous Cell Carcinoma of Ampulla of Vater Pancreatic Somatostatinoma Neurodevelopmental Disorder with Microcephaly - Seizures and Cortical Atrophy Defect in Transport of Long Chain Fatty Acids Duodenal Somatostatinoma Cavernous Hemangioma of the Face Mixed Fibrolamellar Hepatocellular Carcinoma Absence of Gluteal Muscles Refractory Hematologic Cancer Basophilic Adenocarcinoma Brain Dopamine-Serotonin Vesicular Transport Disease Gonococcal Keratitis Polyomavirus-Associated Nephropathy Pechet Factor Deficiency Cryptogenic Late-Onset Epileptic Spasms Intellectual Developmental Disorder - Dysmorphic Facies - Behavioral Abnormalities Intranuclear Rod Myopathy TSEN54-Related Pontocerebellar Hypoplasia Frontal Sinus Neoplasm Plasmacytoid Urothelial Carcinoma Central Nervous System Fibrosarcoma Urethral False Passage Ossified Ear Cartilages Benign Perivascular Tumor Parainfluenza Virus Type 3 Uterine Corpus Choriocarcinoma Supraglottic Laryngeal Cancer Pediatric Infratentorial Ependymoblastoma Papillary Cystadenoma of Uterine Ligament Chromosome 17p Deletion Mold-Related Illness Focal Segmental Glomerulosclerosis Type 1 Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase Gonococcal Bursitis Sacral Chordoma Epileptic Hemiplegia Electroclinical Syndrome Deep Corneal Vascularisation Sickle Delta Beta Thalassemia Scn9a-Related Inherited Erythromelalgia Combined Oxidative Phosphorylation Deficiency 29 Paraurethral Gland Neoplasm Congenital Deafness with Total Albinism Scirrhous Breast Carcinoma Ovarian Primitive Germ Cell Tumor Ampulla of Vater Mucinous Adenocarcinoma Congenital Heart Defects and Skeletal Malformations Syndrome Familial Erythrocytosis 6 Malignant Cardiac Germ Cell Tumor Childhood Non-Hodgkin Lymphoma Anterior Scleritis Isolated Ventriculo-Arterial Discordance Aleutian Mink Disease Sphenoid Sinus Schneiderian Papilloma Desmoplastic Infantile Astrocytoma Sweat Gland Neoplasm Cheirospondyloenchondromatosis Kaolin Pneumoconiosis Subglottis Verrucous Carcinoma Squamous Cell Carcinoma of Liver and Intrahepatic Biliary Tract Pediatric Osteosarcoma Unilateral Loss of Labyrinthine Reactivity Prolactin Deficiency with Obesity and Enlarged Testes Pituitary Dwarfism with Large Sella Turcica Alcuronium Bromide Allergy Cutaneous Lipoma Medial Cranial Fossa Meningioma Isolated Congenital Hepatic Fibrosis Congenital Vagal Hyperreflexivity Adult Cystic Teratoma PACS1-Related Syndrome Postlingual Non-Syndromic Genetic Deafness Lacrimal Gland Adenoid Cystic Carcinoma Cervical Mucinous Adenocarcinoma Endocervical Type Autism with Facial Nevus Flammeus Signet Ring Cell Adenocarcinoma of the Prostate Water-Clear Cell Adenoma Papillary Adenoma of the Extrahepatic Bile Duct Familial Localized Heat Urticaria Chronic Myocardial Ischemia Wilms Tumor of the Ovary Aniseikonia Cervical Endometrioid Adenocarcinoma Childhood Central Nervous System Germ Cell Tumor Euryblepharon Pericanalicular Breast Fibroadenoma Uterine Cervix Papillary Carcinoma Pineal Region Yolk Sac Tumor Mediastinal Neurofibroma Brain Sarcoma Disorders with Deficiency of a Single Peroxisomal Enzyme 9q21.13 Microdeletion Syndrome Small Cell Osteogenic Sarcoma Malignant Leydig Cell Tumor of the Testis Pseudoacromegaly with Severe Insulin Resistance Aerobic Actinomyces Infection Hypoganglionosis Abdominal Tuberculosis Sarcoid Meningitis Periampullary Adenocarcinoma POLG-Related Disorder Eyelid Hypopigmentation Corneal Argyrosis Aortic Angiosarcoma Cerebellar Papillary Meningioma Lacrimal Passage Granuloma Brittle Diabetes Central Nervous System Benign Neoplasm Chronic Venous Leg Ulcers Mucinous Adenocarcinoma of the Prostate Pelvic Lipomatosis with Crossed Renal Ectopia Childhood Ovarian Endodermal Sinus Tumor Spigelian Hernia-Cryptorchidism Syndrome Cobblestone Retinal Degeneration Vulvar Syringoma Bartholin Gland Small Cell Carcinoma Rectal Rhabdomyosarcoma Familial Pachydermodactyly Breast Rhabdomyosarcoma Early-Onset Progressive Encephalopathy with Brain Atrophy and Spasticity Dental Fluorosis Cerebellar Hypoplasia Tapetoretinal Degeneration Hypophosphatemic Bone Disease Brain Stem Angioblastoma Liver Fibrosarcoma Die Smulders Vles Fryns Syndrome Facial Nerve Neoplasm Orbit Embryonal Rhabdomyosarcoma Supranuclear Ocular Palsy Renal Pelvis Inverted Papilloma Juvenile Recurrent Parotitis Esophageal Adenoid Cystic Carcinoma Gallbladder Small Cell Carcinoma Chronic Polyradiculoneuritis Esophageal Carcinoma in Situ Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-Ketoglutarate Familial Glomangioma Large Intestine Lipoma MED13L Haploinsufficiency Syndrome Adenosquamous Gallbladder Carcinoma Alveolar Vulvar Soft Part Sarcoma Melanotic Neuroectodermal Tumor Mitochondrial Complex III Deficiency X-Linked Recessive Corpus Callosum Dysgenesis Mesenchymal Glioblastoma Unilateral Retinoblastoma Huntington's Disease-Like Syndrome Methotrexate-Associated Lymphoproliferation Breast Papillomatosis Radiation-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome Sympathetic Neurilemmoma Autosomal Dominant Progressive External Ophthalmoplegia Febrile Ulceronecrotic Mucha-Habermann Disease Spastic Pseudosclerosis Sarcomatoid Uterine Corpus Endometrioid Adenocarcinoma Uterine Corpus Adenocarcinofibroma Angiomyoma Nipple Carcinoma Hypertrophic Olivary Degeneration Mature Ovarian Teratoma Ciliary Body Mixed Cell Melanoma Ragweed Sensitivity Mucinous Intrahepatic Cholangiocarcinoma Endotheliitis Bruyn Scheltens Syndrome Posterior Uveal Melanoma Endometrial Stromal Tumor Insulin-Dependent Diabetes Mellitus 13 Auricular Cancer ITK Deficiency Esophageal Squamous Cell Papilloma Basosquamous Carcinoma Capillary Lymphangioma Fallopian Tube Adenomatoid Tumor Lipid Rich Breast Carcinoma Clear Cell Chondrosarcoma Fallopian Tube Serous Adenocarcinoma Sedoheptulokinase Deficiency Cerebral gigantism associated with Jaw cyst Basal cell Naevoid syndrome Liver Leiomyoma Breast Apocrine Adenoma Alcoholic Psychosis Testicular Microlithiasis Brachydactyly Type E with Atrial Septal Defect Type 2 Central Nervous System Calcification-Deafness-Tubular Acidosis-Anemia Syndrome Chromosome 21q Deletion External Ear Carcinoma Adult Central Nervous System Immature Teratoma Chromosome 1p35 Deletion Syndrome Nonsyndromic Hearing Loss and Deafness DFNA3 Congenital Muscular Dystrophy with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers Familial Stomach Cancer Spinal Polio Sphenoidal Sinus Neoplasm Splenic Flexure Cancer Acute Salpingo-Oophoritis Panic Disorder 3 Isolated Agenesis of the Gallbladder Gallbladder Carcinoma in Situ Neonatal Group B Streptococcal Infection Neuroendocrine Tumor of the Middle Ear Intellectual Disability - Athetosis - Microphthalmia Chronic Gonorrhea of the Cervix Adult Malignant Schwannoma Autosomal Recessive Spastic Ataxia 8 with Hypomyelinating Leukodystrophy Familial Capillaro-Venous Leptomeningeal Angiomatosis AP4 Deficiency Syndrome Benign Neoplasm of the Fallopian Tube Carabelli Anomaly of the Maxillary Molar Teeth Ovarian Squamous Cell Carcinoma Glossopalatine Ankylosis - Micrognathia - Ear Anomalies Plexopathy Major Depressive Disorder 1 Pseudoangiomatous Stromal Hyperplasia Penile Verrucous Carcinoma Uncombable Hair Syndrome 3 Hypomyelinating Leukodystrophy Type 12 Idiopathic Generalized Epilepsy 15 Cleavage of Iris Pigment Layer Ethanolaminosis KCNQ3-Related Disorder Basaloid Squamous Cell Carcinoma Ischemic Retinopathy Gallbladder Lymphoma Cerebellar Medulloblastoma Familial Antiphospholipid Syndrome Exhibitionism Alopecia Universalis - Onychodystrophy - Vitiligo Adenocarcinoma of the Ureter Lymphoepithelioma-Like Thymic Carcinoma Laryngeal Verrucous Carcinoma Postgerminal Center Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 6-Phosphogluconolactonase Deficiency Double Inguinal Hernia Pseudometachromatic Leukodystrophy Diffuse Leptomeningeal Melanocytosis Frontal Convexity Meningioma Cryofibrinogenemia Snatiation PPP2R5D-Related Neurodevelopmental Disorder Intermediate Malignant Teratoma Congenital Anomalies of Kidney and Urinary Tract with or without Hearing Loss - Abnormal Ears - Developmental Delay Lymph Node Adenoid Cystic Carcinoma Mediastinal Seminoma Uterine Corpus Epithelioid Leiomyoma Childhood Renal Cancer Cribriform Carcinoma Autosomal Dominant Chronic Granulomatous Disease Branchial Myoclonus - Spastic Paraparesis - Cerebellar Ataxia Trochlear Dysplasia Kyphoscoliosis 1 Autosomal Dominant Nonsyndromic Deafness 72 Glottic Verrucous Carcinoma Intrahepatic Bile Duct Cystadenoma Familial Transverse Nasal Groove Global Developmental Delay with or Without Impaired Intellectual Development Airway-Centered Interstitial Fibrosis Childhood Malignant Hemangiopericytoma Angioosteohypotrophic Syndrome Ventilator-Induced Diaphragmatic Dysfunction Sclerosing Perineurioma Infantile Spasms - Psychomotor Retardation - Progressive Brain Atrophy - Basal Ganglia Disease Skeletal Dysplasia - Orofacial Anomalies Cysteine Peptiduria Female Infertility due to Oocyte Meiotic Arrest Splenic Manifestation of Prolymphocytic Leukemia Rectosigmoid Cancer Peripheral Nerve Hemangioma Non-Herpetic Acute Limbic Encephalitis Papillary Kidney Adenoma Type 2 Ductal Breast Carcinoma Peripheral Arterial Occlusive Disease 1 Extraneural Perineurioma Benign Ureteral Neoplasm Chronic Relapsing Inflammatory Optic Neuropathy Colorectal Sarcoma Mucinous Adenofibroma Catsper-Related Male Infertility Hypomyelinating Leukodystrophy Type 10 Sclerosing Hepatic Carcinoma Melanomatosis Cardiomyopathy Associated with Myopathy and Sudden Death Non-Papillary Transitional Cell Carcinoma of the Bladder Chlorhexidine Allergy Hidradenocarcinoma Syringomas - Natal Teeth - Oligodontia Verrucous Squamous Cell Carcinoma of the Bladder Autoimmune-Related Retinopathy and Optic Neuropathy Pulmonary Sclerosing Hemangioma Primary Progressive Freezing Gait Melphalan Allergy Anal Gland Adenocarcinoma Deficient N-Hydroxylation of Amobarbital IRF6-Related Disorder External Resorption of Tooth Acquired Hemophagocytic Lymphohistiocytosis Associated with Malignant Disease Heart Leiomyosarcoma Nonsyndromic Hearing Loss and Deafness DFNB1 Lobomycosis Congenital Hypopituitarism with Central Diabetes Insipidus Rete Ovarii Cystadenofibroma Lower Clivus Meningioma Factor V Excess with Spontaneous Thrombosis Autosomal Dominant Mental Retardation 49 Adult Central Nervous System Germ Cell Tumor Foramen Magnum Meningioma Secretory Diarrhea - Myopathy - Deafness Separation Anxiety Disorder Mucinous Adenocarcinoma Prostate Lymphoma Benign Cardiovascular Organ Neoplasm Nonsyndromic Retinitis Pigmentosa Dysbaric Osteonecrosis Ataxia - Photosensitivity - Short Stature Chromosome 15q25 Deletion Syndrome Solar Retinopathy Jejunal Atresia with Renal Adysplasia Malignant Pheochromocytoma Green Sandford Davison Syndrome Mild Androgen Insensitivity Syndrome Retroperitoneal Hemangiopericytoma Mucinous Eccrine Carcinoma CHD2-Related Neurodevelopmental Disorder Cold-Induced Sweating Syndrome Amyotrophic Choreoacanthocytosis Fallopian Tube Endometrioid Adenocarcinoma Platelet Prostacyclin Receptor Defect Childhood Small Intestinal Cancer Bile Duct Rhabdomyosarcoma ISCA2-Related Mitochondrial Disorder Dermoid Cyst of the Skin Polyembryoma of the Ovary Fucosyltransferase 6 Deficiency Benign Infantile Seizures Associated with Mild Gastroenteritis Lymphoplasmacytic Lymphoma Without IgM Production Conjunctival Squamous Cell Carcinoma Early-Onset Progressive Encephalopathy with Brain Atrophy and Thin Corpus Callosum Trombiculiasis Pleural Lipoma Mediastinal Leiomyosarcoma Synchronous Bilateral Breast Carcinoma Marantic Endocarditis Teratoma with Malignant Transformation Plum Allergy Diffuse Uterine Corpus Leiomyomatosis Tenosynovitis of Foot and Ankle Behcet Disease Arthropathy Rete Testis Adenoma Bacterial Exanthem Bacterial Gastritis Hydrocephalus - Obesity - Hypogonadism Myocardial Infarction Type 2 Childhood Breast Cancer Medium Chain 3-Ketoacyl-Coa Thiolase Deficiency Monoclonal Mast Cell Activation Syndrome Adult Leptomeningeal Melanoma Chronic Active Epstein-Barr Virus Infection Glaucoma Type 1C Internal Auditory Canal Meningioma Spastic Paraplegia - Optic Atrophy - Dementia Pulmonic Stenosis - Congenital Nephrosis Bednar Tumor Bile Duct Mucoepidermoid Carcinoma Rotation of Upper Central Incisors Proliferative Fasciitis Male Infertility due to Acephalic Spermatozoa Vaginal Squamous Papilloma X-Linked Hereditary Ataxia Congenital Brachyesophagus - Intrathoracic Stomach - Vertebral Anomalies Focal Epithelial Hyperplasia of Schock Spinal Cord Astrocytoma External Auditory Meatus Lipoma Benign Respiratory Tract Neoplasm Segmental Dystonia Mucinous Lung Adenocarcinoma Ovarian Liposarcoma Hereditary Persistence of Fetal Haemoglobin - Beta Thalassaemia Metastatic Melanoma Acute Conjunctivitis Rhizomelic Osteochondrodysplasia with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension Combined Oxidative Phosphorylation Deficiency 31 Small Intestine Diverticulitis Colonic Varices without Portal Hypertension Anal Rhabdomyosarcoma Autosomal Recessive Erythropoietic Protoporphyria Benign Intestinal Neuroendocrine Tumor Hepatoid Adenocarcinoma Interferon-Gamma Receptor 1 Deficiency Mucosal Melanoma Cerebral Artery Occlusion Cervical Spina Bifida Aperta Benign Uterine Neoplasm Tracheal Carcinoma in Situ Cotyledonoid Dissecting Leiomyoma Cohen Lockood Wyborney Syndrome Hypomyelinating Leukodystrophy Type 17 Glandular-Alveolar Pattern Testicular Yolk Sac Tumor X-Linked Mental Retardation Type 106 Harel-Yoon Syndrome Urethral Nephrogenic Adenoma Gallbladder Rhabdomyosarcoma Familial Gastric Neuroendocrine Tumor Type 1 Stenosis of the Lacrimal Sac Autosomal Recessive Congenital Stationary Night Blindness Schizophrenia Type 8 Paraneoplastic Uveitis Cervicomedullary Junction Neoplasm X-Linked Mental Retardation Type 103 Urethral Urothelial Papilloma Anal Neuroendocrine Tumor Ovarian Small Cell Carcinoma of Pulmonary Type Small Cell Carcinoma of the Prostate Ventruto Digirolamo Festa Syndrome Familial Broad Terminal Phalanges Mucinous Nevus Dental Pulp Erosion Cutaneous Meningioma Chronic Polyneuropathy Chronic Angle Closure Glaucoma Severe Juvenile Arteriosclerosis Adenocarcinoma of the Epididymis Diaphragmatic Hernia - Short Bowel - Asplenia Lidocaine Allergy Ventricular Extrasystoles with Syncopal Episodes - Perodactyly - Robin Sequence Central Nervous System Leukemia Autoimmune Disease of the Musculoskeletal System Xylosidase Deficiency Diabetic Mastopathy Bone Fibrosarcoma Minor Vestibular Glands Adenoma Hyperlipoproteinemia and Deafness type 2 Anomalous Coracoclavicular Joint Pancreatic Lipomatosis and Duodenal Stenosis or Atresia in Children Defect of Tricarboxylic Acid Cycle Parasitic Conjunctivitis Vulvar Granular Cell Tumor Urinary Bladder Inverted Papilloma Acute Necrotizing Encephalopathy Ascending Colon Cancer Colon Cavernous Hemangioma Succinate-CoA Ligase Deficiency Androgenetic Alopecia 3 Neonatal Self-Limited Primary Hyperparathyroidism with Hypercalciuria Signet Ring Cell Intrahepatic Cholangiocarcinoma Skin Basaloid Squamous Cell Carcinoma Infiltrating Renal Pelvis and Ureter Transitional Cell Carcinoma Ververi-Brady Syndrome Gata1-Related X-Linked Cytopenia Pediatric Ependymoma Woronets Trait Epidermal Appendage Tumor Neuroendocrine Cell Hyperplasia of Infancy Fenton Wilkinson Toselano Syndrome Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia Pulmonary Meningioma Genetic Mitochondrial Disorders Mixed Cell Type Wilms' Tumor Giant Breast Fibroadenoma Chronic Tubulointerstitial Nephropathy Childhood Embryonal Testis Carcinoma Noninfectious Dermatoses of Eyelid Testicular Thecoma Benign Recurrent Vertigo 2 Familial Hydroa Vacciniforme Progesterone-Receptor Positive Breast Cancer Hepatic Vascular Disorders Sodium-Potassium-Atpase Activity of Red Cell Thyroid Isthmus cancer X-Linked Graves Disease 1 Ovarian Serous Adenofibroma Cervical Mucinous Adenocarcinoma Shih-Filkins Syndrome Chronic Perichondritis of the Pinna Myofibroblastoma of the Breast Craniosynostosis - Contractures - Cleft Submucous Uterine Fibroid Age-Related Macular Degeneration 6 Chronic Tubotympanic Suppurative Otitis Media Congenital Myopathy with Fast-Twitch Fiber Atrophy Levator-Medial Rectus Synkinesis Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities Chromosome 16q Deletion Drug-Induced Hearing Loss Chief Cell Adenoma Jugular Foramen Meningioma Time Agnosia Juvenile Familial Leg Ulcers Twinning Due to Superfetation Adult Mesenchymal Chondrosarcoma Middle Ear Osteoma Zuska Disease Chromosome 19p Deletion Mesenteric Vascular Occlusion Duodenal Adenoma Bone Mineral Density Quantitative Trait Locus 14 Diffuse Infiltrative Lymphocytosis Syndrome Descending Colon Cancer Occult Lung Squamous Cell Carcinoma Childhood Bladder Cancer Variation in Apocrine Gland Secretion Residual Stage Angle-Closure Glaucoma Spongiotic Dermatitis Adult Central Nervous System Choriocarcinoma Cervical Vertebral Bridge Laryngeal Mucoepidermoid Carcinoma Pulmonic Stenosis, Atrial Septal Defect, and Unique Electrocardiographic Abnormalities Central Gyrate Choroidal Dystrophy Female Breast Upper-Inner Quadrant Cancer Oral Tuberculosis Succinylcholine Allergy Adult Endodermal Sinus Tumor Hereditary Sensory and Autonomic Neuropathy Type 8 Variation in Skin/Hair/Eye Pigmentation 9 Perisylvian Polymicrogyria with Cerebellar Hypoplasia and Arthrogryposis Experimental Autoimmune Encephalomyelitis Spastic Paraplegia with Extrapyramidal Signs Giant Cell Granuloma Inner Ear Cancer Ectodermal Dysplasia Type Bartalos Torus Palatinus and Torus Mandibularis Bladder Leiomyoma Multiple Mitochondrial Dysfunctions Syndrome Type 5 Pediatric Renal Cell Carcinoma Pseudohermaphrodism with Anorectal Anomalies Band-Shaped Spheroid Corneal Degeneration Vulvar Seborrheic Keratosis Vulvar Keratoacanthoma-Like Carcinoma Chest Wall Lymphoma Papillary Adenocarcinoma of the Extrahepatic Bile Duct Cobalt Allergic Contact Dermatitis Pediatric Leptomeningeal Melanoma Noninvasive Malignant Thymoma PINK1 Type of Young-Onset Parkinson Disease Luxation of the Globe Elevated Adenosine Triphosphate of Erythrocytes Familial Transverse Nasal Hyperpigmentation Multinodular Goiter 3 Bilateral Choroidal Osteoma Fibrosarcomatous Osteosarcoma Cefuroxime Allergy Sebaceous Adenoma Multilocular Clear Cell Renal Cell Carcinoma Abnormal Glucagon Secretion Rigid Spine Cardiomyopathy Malignant Mediastinal Lymphoma Malignant Sertoli-Leydig Cell Tumor Leiomyoma of the Ureter Arthrogryposis Multiplex Congenita CNS Calcification Serous Cystadenocarcinoma Phosphohydroxylysinuria Benign Mediastinal Psammomatous Neurilemmoma Autosomal Dominant Preaxial Polydactyly - Upperback Hypertrichosis Syndrome GRIN2B-Related Syndrome Hypermanganesemia with Dystonia Spastic Tetraplegia - Thin Corpus Callosum - Progressive Postnatal Microcephaly Tracheal Mucoepidermoid Carcinoma Brachydactyly Type A2 with Microcephaly Supratentorial Embryonal Tumor of Childhood Fibrogenesis Imperfecta Ossium Glutamyl Ribose-5-Phosphate Storage Disease Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport Testicular Gonadoblastoma Bilateral Hypoactive Labyrinth Dupont Sellier Chochillon Syndrome Bulbomembranous Urethral Cancer Mesenteric Artery Occlusion Insulin-Dependent Diabetes Mellitus 15 Hypoproteinemic Edema Acute Sarcoidosis Pigmentary Retinopathy Acute Coronary Syndrome Wound Kounis Syndrome Supination Injury Injury Complete Locked-in Syndrome Xanthelasma Middle East Respiratory Syndrome Atypical Absence Seizure Focal Onset Aware Seizure Epilepsy with Generalized Tonic Clonic Seizures Alone Spinal Trauma Inverse Psoriasis Penile Intraepithelial Neoplasia Pearly Penile Papules Zoon Balanitis Febrile Neutropenia Upper Airway Cough Syndrome Immune Complex–Mediated Small Vessel Vasculitis Papillary Serous Cystadenocarcinoma of the Ovary Autoimmune Gastritis Acute Chest Syndrome Terminal 4q Deletion Syndrome ARDS Clinical Musculoskeletal Lower Back Pain Recurrent Pyogenic Cholangitis Serratia Enterobacter Streptococcus Viridans Methicillin-resistant Staphylococcus Aureus Proteus Acetinobacter Morganella Morganii Citrobacter Paragonimus Uterobilateralis Trichobilharzia Regenti Schistosoma Mekongi Thelazia Californiensis Plasmodium Ovale Rhinosporidium Seeberi Hymenolepis Diminuta Clonorchis Viverrini Anisakis Metagonimus Yokogawai Paragonimus Skrjabini Cochliomyia Hominivorax Loa Loa Filaria Plasmodium Vivax Plasmodium Knowlesi Opisthorchis Viverrini Linguatula Serrata Trichinella Nelsoni Balantidium Coli Schistosoma Haematobium Balamuthia Mandrillaris Trypanosoma Brucei Dermatobia Hominis Halicephalobus Gingivalis Mansonella Streptocerca Babesia Metorchis Conjunctus Onchocerca Volvulus Fasciola Gigantica Trichinella Britovi Schistosoma Intercalatum Brugia Timori Trichinella Nativa Opisthorchis Felineus Dracunculus Medinensis Hymenolepis Nana Archiacanthocephala Schistosoma Enterobius Vermicularis Dioctophyme Renale Bertiella Mucronata Leishmania Sarcocystis Suihominis Clonorchis Sinensis Naegleria Fowleri Baylisascaris Procyonis Dientamoeba Fragilis Cryptosporidium Angiostrongylus Costaricensis Enterobius Gregorii Trichuris Vulpis Paragonimus Africanus Trichomonas Vaginalis Spirometra Erinaceieuropaei Bertiella Studeri Paragonimus Kellicotti Schistosoma Japonicum Trichuris Trichiura Thelazia Callipaeda Tunga Penetrans Paragonimus Caliensis Dicrocoelium Dendriticum Acanthamoeba Autoimmune Pangastritis Leptomeningeal TTR Amyloidosis TTR Amyloidosis with Cardiomyopathy Banna Virus Coltivirus Rotavirus Rabies Virus Mumps Rubulavirus Measles Virus Marburg Virus Ebola Virus Hantaan Virus Crimean-Congo Hemorrhagic Fever Virus Lassa Virus Influenza Virus Human Immunodeficiency Virus Hepatitis E Virus Tick-Borne Encephalitis Virus West Nile Virus Dengue Virus Yellow Fever Virus Hepatitis C Virus Severe Acute Respiratory Syndrome Virus Poliovirus Hepatitis A Virus Norwalk Virus Hepatitis B Virus JC Virus BK Virus Herpes Simplex Virus 2 Infection Herpes Simplex Virus 1 Infection Adenovirus Papillomaviridae Micrococcus Luteus Mycobacterium Avium Salmonella Typhimurium Mycoplasma Pneumoniae Bacillus Licheniformis Mycoplasma Penetrans Bordetella Streptococcus Lactis Staphylococcus Lactobacillus Acidophilus Brucella Melitensis Staphylococcus Epidermidis Streptococcus Ferus Streptococcus Faecalis Enterococcus Faecalis Mycobacterium Leprae Chlamydophila Psittaci Burkholderia Neisseria Bacillus Megaterium Neisseria Meningitidis Clostridium Botulinum Campylobacter Coli Microbacterium Multiforme Streptococcus Sanguis Mycobacterium Intracellulare Anaplasma Bacillus Thuringiensis Chlamydophila Mycobacterium Phlei Streptococcus Gallinarum Streptococcus Mitior Streptococcus Salivarius Streptococcus Pasteurella Anaplasma Phagocytophilum Campylobacter Jejuni Bacillus Brevis Streptococcus Rattus Mycoplasma Genitalium Campylobacter Streptococcus Mutans Methanobacterium Extroquens Streptococcus Agalactiae Enterococcus Galllinarum Agrobacterium Tumefaciens Enterobacter Cloacae Streptococcus Pyogenes Streptococcus Avium Haemophilus Influenzae Enterococcus Maloratus Bacteroides Lactobacillus Bacillus Subtilis Mycoplasma Fermentans Brucella Porphyromonas Gingivalis Acetobacter Aurantius Enterococcus Faecium Azotobacter Vinelandii Bacillus Stearothermophilus Lactobacillus Casei Bacillus Cereus Mycobacterium Streptococcus Cricetus Spirillum Volutans Enterococcus Durans Escherichia Coli Azorhizobium Caulinodans Haemophilus Bacillus Fusiformis Rothia Dentocariosa Streptococcus Sobrinus Pasteurella Multocida Bacillus Anthracis Corynebacterium Bacillus Lactobacillus Bulgaricus Peptostreptococcus Mycobacterium Tuberculosis Clostridium Tetani Enterococcus Avium Bordetella Bronchiseptica Treponema Denticola Lactococcus Lactis Bacillus Mycoides Treponema Mycobacterium Smegmatis Campylobacter Fetus Salmonella Enteritidis Vibrio Fusobacterium Nucleatum Burkholderia Cepacia Mycobacterium Lepraemurium Streptococcus Oralis Gardnerella Vaginalis Vibrio Cholerae Wolbachia Yersinia Yersinia Pestis Yersinia Pseudotuberculosis Herpes Simplex Virus Type 1 Minimally Conscious State Childhood Gastric Carcinoma Childhood Soft Tissue Sarcoma ROHHAD Syndrome Pheochromocytoma in Childhood Peripheral T-cell Lymphoma Methylmalonic Acidemia with Homocystinuria Malignant Melanoma in Childhood Duodenal Carcinoid Syndrome CDK4-linked Melanoma BRCA2-Associated Hereditary Breast and Ovarian Cancer Syndrome BRCA1-Associated Hereditary Breast and Ovarian Cancer Syndrome Primary Malignant Melanoma of the Conjunctiva Pheochromocytoma-Islet Cell Tumor Syndrome Pediatric Ulcerative Colitis Pediatric Hypertension Pediatric Crohn Disease Parkinson's Disease Type 3 Epithelial Ovarian Cancer Childhood Non-Small Cell Lung Cancer Merkel Cell Carcinoma Hereditary Renal Cell Carcinoma Hereditary Orotic Aciduria without Megaloblastic Anemia Ewing Family of Tumors Endemic Kaposi Sarcoma Disseminated Infection with Mycobacterium Avium Complex Digestive System Melanoma Cardiomyopathy due to Anthracyclines Childhood Carcinoid Tumor Acute Myeloid Leukemia with Myelodysplasia-related Changes ALK+ Histiocytosis Acquired Hemophilia A Diffuse Intrinsic Pontine Glioma Caudal Dysplasia Syndrome Panencephalitis Pelvic Organ Prolapse Injury of Anus Hypoxic-Ischemic Brain Injury Skeletal Injury