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Wedge Defect of Tooth Absolute Glaucoma Bowenoid Papulosis Irons-Bhan Syndrome Oropharyngeal Carcinoma Davis-Lafer Syndrome Partial Trisomy 18q Low T3 Syndrome Pathophobia Macular Cutaneous Amyloidosis Cannabis Withdrawal Trifoliate Orange Poisoning Genital Psoriasis Rowley-Rosenberg Syndrome Trichosporon Inflammatory Bowel Disease Type 6 Steroid Abuse Schizophrenia Type 11 Aase Syndrome Allodynia Tonsillar-Pharyngeal Diphteria Angioma of the Lip Noctiphobia Hyperemia Palant Cleft Palate Syndrome Hypnic Jerk Borries Syndrome Periventricular Laminar Heterotopia Wallerian Degeneration Follicular Large-Cell Lymphoma Sakamoto Disease Zephyranthes Atamasco Poisoning Hereditary Spherocytosis Type 2 Thomas-Jewett-Raines Syndrome Chondritis Acute Stress Disorder Akaba-Hayasaka Syndrome Phorate Poisoning Roseola Infantum Submandibular Gland Adenocarcinoma Bernheim Syndrome Chondromatosis Plica Syndrome Drug-Induced Sideroblastic Anemia Wisconsin Syndrome Local Anaesthetic Allergy Inflammatory Bowel Disease Type 9 Staphylococcal Toxic Shock Syndrome Acute Hepatitis B Insect Allergy Hyperosmolar Hyperglycemic Non-Ketotic Syndrome Molybdenum Deficiency Type A Influenza Subtype H1N2 Inflammatory Bowel Disease Type 10 Taijin-Kyofusho Syndrome Hyperandrogenism Acute Lymphoblastic Leukemia Type L1 Intervertebral Disc Disease Silent Myocardial Infarction Mumps-Associated Pancreatitis Cone Shell Poisoning Navajo Poikiloderma Hypertrophic Subaortic Stenosis Macrocytic Hyperchromic Anemia Susceptibility to Celiac Disease 9 Schizotypal Personality Disorder Goldstein-Hutt Syndrome Ramsay-Hunt Cerebellar Syndrome Laryngitis Jatropha Multifida Poisoning Mirizzi Syndrome Isospora Belli Infection Susceptibility to Celiac Disease 6 Pseudoinflammatory Fundus Dystrophy Alveolar Periostitis Autoimmune Disease of the Nervous System Oral Squamous Cell Carcinoma Stage 4 Atypical Rett Syndrome Respiratory Sounds Pointer Syndrome Acephalgic Migraine Ziprkowski-Margolis Syndrome Nasal-Type Extranodal NK-T-Cell Lymphoma Stage 3 Space Adaptation Syndrome Infantile Apnea Adrenal Hypertension Congenital Symmetric Circumferential Skin Creases Type 1 Acute Hepatitis D Excoriated Acne Chronic Pharyngitis Macrognathism Laurence-Prosser-Rocker Syndrome Opium Addiction Acute Hepatitis A Vascular Malformations of the Brain Vitamin C Deficiency Submandibular Gland Carcinoma Traumatic Laryngitis Nodular Scleritis Globulomaxillary Cyst Aspergillus Niger Infection Burnett-Schwartz-Berberian Syndrome Complex Migraine Trisomy 3 Large Cell Carcinoma Hereditary Sensory and Autonomic Neuropathy Type 2 Mansonella Ozzardi Infection Dipylidiasis Mosaic Trisomy 17 Shwartzman Phenomenon Accessory Navicular Bone Tang Hsi Ryu Syndrome Hypopharyngeal Tumor Benign Oral Neoplasm Glassy Cell Carcinoma of the Cervix Heroin Overdose Lantana Poisoning Jeune-Tommasi Syndrome Partial Trisomy 10q Faye-Petersen-Ward-Carey Syndrome Acute Hepatitis E Contact Dermatitis due to Drugs Catarrh Ecstasy Overdose Primary Insomnia Angioma Ameloblastic Fibroma Bowel Bypass Syndrome Bronze Baby Syndrome Gullner Syndrome Herpes Simplex Keratitis Camera-Marugo-Cohen Syndrome Aquired Fibrokeratoma Iliohypogastric Nerve Disorder Notalgia Paresthetica Adenocarcinoid Tumor Lateral Periodontal Cyst Rectal Abscess Posthemorrhagic Hydrocephalus Cutaneous Necrotizing Vasculitis Methylene Chloride - Occupational Liver Damage Acute Congestive Hepatopathy Cherry Laurel Poisoning Spinal Dural Arteriovenous Fistula Trisomy 13q Fistula Blegvad-Haxthausen Syndrome Follicular Cyst Anorectal Atresia Ectopic Acromegaly Pyrrolizidine Alkaloids Poisoning Schizophrenia Type 5 Invasive Breast Cancer Partial Monosomy 11q Pulmonary Sarcoidosis Type 3 Corneal Endothelial Dystrophy Type 1 Senile Retinoschisis Familial Paget Disease of Bone Genitofemoral Nerve Disorder Colonic Inertia Autophobia Intestinal Duplication Leg Injury Inflammatory Bowel Disease Type 21 Fungal Infection of Hair Silicosiderosis Benign Tongue Neoplasm Shaken Baby Syndrome Coral Bean Poisoning Toxic Pulmonary Edema Exercise-Induced Asthma Pancoast Tumor Erythroderma Desquamativa of Leiner Lymphatic Obstruction Immunoproliferative Diseases Hyperoxia Tulip Poisoning Kasznica-Carlson-Coppedge Syndrome Cardiogenic Pulmonary Edema Marijuana Addiction Kuster Syndrome Ovarian Remnant Syndrome Neurasthenia Nephritic Syndrome Chronic Ulcerative Pulpitis Digital Flexor Tendon Rupture Borderline Personality Disorder Lidocain Poisoning Oral Squamous Cell Carcinoma Pharmacophobia Finger Arthritis Dieterich's Disease Chromosome 6q Duplication Syndrome Bacterial Pericarditis TAU Syndrome Bartter Syndrome Type 4 Maple Syrup Urine Disease Type 2 Chlorodontia Oculo-Oto-Facial Dysplasia Lymphatic System Tumors Repetitive Strain Injury Darvocet Withdrawal Trueb-Burg-Bottani Syndrome Acute Hepatitis C Telencephalic Leukoencephalopathy Childhood Hodgkin Lymphoma Hemorrhoids Grade 4 Benign Multiple Sclerosis Acute Viral Bronchiolitis Anterior Interosseous Nerve Disorder Actinic Cheilitis Myopia Type 2 Selective Mutism Flea-Borne Infectious Diseases Cat Allergy Post-Traumatic Epilepsy Pseudoainhum Partial Monosomy 13q Agyrophobia Thirst Fever Hooft Disease Multicentric Reticulohistiocytosis Scapulocostal Syndrome Partial Trisomy 15q Calculi Infantile Gluteal Granuloma Partial Trisomy 9p Disulfiram Poisoning Nodular Sclerosing Classical Hodgkin Lymphoma Toe Arthritis Asymmetric Short Stature Syndrome Palate Cancer Monosomy 2q Brainstem Auditory Evoked Responses Connatal Pelizaeus-Merzbacher Disease Cold Skin Descending Perineum Syndrome Amaurosis Fugax Zinc Poisoning Megalocytic Interstitial Nephritis Type A Influenza Subtype H9N2 Narcolepsy without Cataplexy Ameloblastic Fibro-Odontosarcoma Cathinone Poisoning Glycoprotein Storage Disease Selig-Benacerraf-Greene Syndrome Microspherophakia with Hernia Eastern Brown Snake Poisoning Connective Tissue Nevus Bing-Neel Syndrome Essential Thrombocytopenia May-White Syndrome Arcobacter Cryaerophilus Infection Kappa Light Chain Myeloma Anisometropia Myopathic Carnitine Deficiency Acquired Hypothyroidism Eosinophilic Synovitis Hepatic Jaundice Aflatoxin B1 Karandikar-Maria-Kamble Syndrome Acquired Lactase Deficiency Wandering Spleen Amlodipine Fournier Gangrene Berlin Syndrome Microphobia Devriendt Syndrome Intraventricular Hemorrhage of the Premature Infant Hypervitaminosis B Complex Familial Hypertrophic Cardiomyopathy Type 3 Trichloroethane - Kidney Damage Iris Hypoplasia and Glaucoma Copper Poisoning 2p12-p11.2 Deletion Syndrome Berk-Tabatznik Syndrome Le Marec-Bracq-Picaud Syndrome Lattice Corneal Dystrophy Type 2 Suppurative Parotitis Inflammatory Bowel Disease Type 20 Odontogenic Carcinosarcoma Ameloblastic Fibro-Odontoma Cardiac Sarcoidosis Charcot-Marie-Tooth Disease Type 2A Iida-Kannari Syndrome Odontophobia Phacolytic Glaucoma Abalone Poisoning Phyllodes Tumor of the Prostate Muller-Barth-Menger Syndrome Duplication of Whole Lower Limb Dehydratase Deficiency Babinski-Nageotte Syndrome Cervicogenic Headache Mansonella Perstans Infection Perianal Thrombosis Steroid Rosacea Quinolone - Drug-Induced Liver Damage Infection with Oesophagostomum Spp. Pudendal Nerve Entrapment Boron Deficiency Abdominal Neoplasm Tabatznik Syndrome Acute Sphenoidal Sinusitis Lupus Nephritis WHO Class 2 Eosinophilic Meningitis Dysmorphophobia Hexane - Chemical Poisoning Abnormal Body Odor Ossifying Fibroma Malignant Tongue Neoplasm Olfactory Nerve Disorder Sublingual Gland Neoplasm Erotophobia Mosquito Bite Visual Pathway Glioma Siderosis Primary Autoimmune Hemolytic Anemia Non-Scarring Alopecia Potato Nose Primary Intraosseous Carcinoma Trisomy 15q Postmenopausal Osteoporosis Colonic Volvulus Primary Biliary Cirrhosis 1 Catarrhal Otitis Media Allen-Masters Syndrome Nodular Malignant Melanoma Superficial Spreading Melanoma Limb-Body Wall Complex Lung Fibroma Osteochondrosis Astley-Kendall Syndrome Hyperkinetic Dysarthria Malignant Eye Neoplasm Transient Osteoporosis of the Hip Human T-Lymphotropic Virus Type 3 X-linked Mental Retardation Type 12 Susceptibility to Celiac Disease 7 Infectious Diarrhea Submandibular Gland Acinic Cell Carcinoma Battaglia-Neri Syndrome Littoral Cell Angioma of the Spleen Tonic Seizure Seghers Syndrome Multiple Myeloma Type IgD Parotid Gland Warthin Tumor Arterial Priapism Nasal Tuberculosis FG Syndrome Type 2 Rape Trauma Syndrome Charcot-Marie-Tooth Disease with Deafness - Mental Retardation - Absence of Large Myelinated Fibers Adult Myxedema Early-Onset Nemaline Myopathy Louse-Borne Diseases Jaffer-Beighton Syndrome Naphthalene Benadryl -- Teratogenic Agent Variant Creutzfeldt-Jakob Disease Gastric Erosion Partial Trisomy 3q Inflammatory Bowel Disease Type 15 Autoimmune Progesterone Dermatitis Brachioskeletogenital Syndrome Autosomal Dominant Polycystic Kidney Disease Type 2 Chronic Venous Insufficiency  Zoophobia Parathyroid Hyperplasia Physical Addiction Paramolar Factor XIII Deficiency Colorectal Polyps Atheroma Dissociated Sensory Loss Coitophobia Adenitis Ventricular Flutter Monosomy 3p Tuberculous Uveitis Malignant Penile Neoplasm Sarcomatoid Mesothelioma Amelogenesis Imperfecta Hypoplastic Type Nutritional Anemia Haptophobia Crumpled Helices and Small Mouth Scapuloperoneal Myopathy Dibasic Aminoaciduria Type 1 Abdominal Cystic Lymphangioma Meningioma 1 Secondary Insomnia Hodgkin Lymphoma during Pregnancy Piperazine -- Teratogenic Agent Trimethylaminuria Spermatophobia Primary Open-Angle Glaucoma Type 1B Death Camas Poisoning Primary Open-Angle Glaucoma Type 1I Granulomatous Cheilitis Schlegelberger-Grote Syndrome Cephalic Disorders Familial Hyperlipoproteinemia Visceral Pain Ulcerative Proctosigmoiditis Chronic Paroxysmal Hemicrania Bacterial Corneal Ulcer Hereditary Nephrotic Syndrome Blitz-Nick-Salaam Attacks Avascular Necrosis of Humerus Diphenoxylate -- Teratogenic Agent Trisomy 12p Valsartan -- Teratogenic Agent Infective Endocarditis Diffuse Neonatal Hemangiomatosis Elbow Injury Heliotrope Poisoning Bone and Cartilage Tumors Carbon Monoxide -- Teratogenic Agent Hypokinetic Dysarthria Gestational Diabetes Partial Monosomy 8q Pelvic Lipomatosis Hypodermyiasis Colorectal Carcinoma Avian Influenza Phototoxic Eczema SAPHO Syndrome Chromosome 7p Duplication Syndrome Twin-Twin Transfusion Syndrome Dilaudid Biliary Disorder Non-Allergic Asthma Posterior Tibial Tendon Rupture Squamous Cell Neoplasm Megaduodenum and/or Megacystis Amnesic Shellfish Poisoning Pulmonary Venous Hypertension Facial Parasthesia Spencer Disease Diverticulosis of the Ileum Hedblom Syndrome Psychological Dependence Bhaskar-Jagannathan Syndrome Lucio Phenomenon Juvenile Tay-Sachs Disease Phenol Sulfotransferase Deficiency Macular Hole Deep Scleritis Premature Aging Type Okamoto Königsmark-Knox-Hussels Syndrome Grasp Reflex Drug-Induced Headache Sea Urchin Poisoning Parotid Gland Carcinoma Sindbis Fever Partial Monosomy 21q Polyphobia FG Syndrome Type 3 Ochlophobia Lymphoblastic Lymphoma Chronic Dacryocystitis Noise-Induced Hearing Loss Laryngopharyngeal Reflux Porcelain Gallbladder Hemolytic Jaundice Helicobacter Cinaedi Infection Perinatal Hypophosphatasia Tollner-Horst-Manzke Syndrome Palpebral Dermoid Cyst Jaw Conditions Isothiazolinone Allergy Sudden Arrhythmic Death Syndrome Arcobacter Butzleri Infection Hemochromatosis Type 2 Parotid Gland Carcinosarcoma Upper Back Sprain Hereditary Factor VII Deficiency Pulsus Bisferiens Dorsiflexion Deformity of Foot Senna Obtusifolia Poisoning Sun Allergy Ribbing Disease Lentigo Maligna Monophobia Juvenile Scleroderma Glucose-Stimulated Secretory Diarrhea - Common Variable Immunodeficiency Uremic Pericarditis Trisomy 4 with or without Mosaicism Hecht Giant Cell Pneumonia in Measles Agenesis of Pulmonary Artery Paroxysmal Nocturnal Dyspnea Bertielliasis Kennerknecht Syndrome Autosomal Dominant Autoimmune Polyendocrine Syndrome Type 1 Charcot-Marie-Tooth Disease Type 1 with Aplasia Cutis Congenita Hypoketonemic Hypoglycemia Achrestic Anemia MSI-H Colorectal Cancer Miliaria Hornova-Dlurosova Syndrome Brachydactyly Type A3 Susceptibility to Celiac Disease 11 Loquat Poisoning Rheumatoid Vasculitis Neuroma Smoldering Adult T-Cell Leukemia Meigel Disease Imerslund-Gräsbeck Syndrome Skunk Cabbage Poisoning AIDS-Related Opportunistic Infections Panophthalmitis Acute Arterial Occlusion Rhinolith Cardiac Compression Syndrome Cramp-Fasciculations Syndrome Ballantyne-Runge Syndrome Trisomy 22q11-q13 Chromosome 1q Duplication Syndrome Bathophobia Chromosome 12p Deletion Syndrome Roy-Maroteaux-Kremp Syndrome Optic Nerve Sheath Meningioma Allergenic Cross-Reactivity Combined Small-Cell Carcinoma Philadelphia Chromosome Negative Chronic Myeloid Leukemia Respiratory Arrest Cherry Laurel Seed Poisoning Gynophobia Pyorrhea Funiculitis Dental Disorder Atropa Belladonna Mechanical Complication of Prosthetic Joint Primary Progressive Multiple Sclerosis Carpal Instability Ligament Tear Rectal Ulceration Internal Joint Prosthesis Broken Missed Abortion Hyperpituitarism Mosaic Trisomy 9 Haddad Syndrome Hemimegalencephaly Anodontia of Permanent Teeth Selective Tooth Agenesis Type 5 Selective Tooth Agenesis Type 3 Selective Tooth Agenesis Type 4 Selective Tooth Agenesis Type 1 Anodontia Subcortical Band Heterotopia Nipah Virus Disease LIG4 Syndrome Autosomal Dominant Myoglobinuria Genetic Recurrent Myoglobinuria Hashimoto-Pritzker Syndrome Primary Parathyroid Hyperplasia Hyperparathyroidism-Jaw Tumor Syndrome Familial Isolated Hyperparathyroidism ACTH-Dependent Cushing Syndrome Gynandroblastoma Chronic Graft-Versus-Host-Disease Streptococcal Toxic-Shock Syndrome Placental-Site Trophoblastic Tumor Gestational Choriocarcinoma Malignant Placental Neoplasm Benign Recurrent Intrahepatic Cholestasis Type 1 Dedifferentiated Liposarcoma Pleomorphic Liposarcoma Well-Differentiated Liposarcoma Klatskin Tumor Apnea of Prematurity Cerebral Amyloid Angiopathy Intraneural Perineurioma Amelogenesis Imperfecta Hypomaturation Type Primary Progressive Non-Fluent Aphasia Semantic Dementia Hereditary Angioedema Type 2 Carcinoid Tumor and Carcinoid Syndrome Autosomal Recessive Spastic Paraplegia Type 25 Peters Anomaly - Cataract Syndrome Familial Hypocalciuric Hypercalcemia Type 2 Spinocerebellar Ataxia Type 22 Metabolic Liver Disease Spotted Fever Rickettsiosis Typhus-Group Rickettsiosis Autosomal Recessive Limb-Girdle Muscular Dystrophy Pure Hereditary Spastic Paraplegia IgG Deficiency Intestinal Polyposis Syndrome Cerebrovascular Dementia Tauopathy Combined Deficiency of Vitamin K-Dependent Clotting Factors Type 2 Combined Deficiency of Vitamin K-Dependent Clotting Factors Type 1 Metabolic Myopathy Idiopathic Inflammatory Myopathy Idiopathic Interstitial Pneumonia Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 3 Congenital Anomaly of the Great Arteries Myopia Type 23 Goniodysgenesis Vitreoretinal Degeneration Optic Atrophy Type 4 Secondary Entropion Congenital Entropion Congenital Upper Palpebral Retraction Palpebral Nevus Syndromic Orbital Border Hypoplasia Conjunctival Lymphangiectasia Adult-Onset Foveomacular Vitelliform Dystrophy Reticular Dystrophy of the Retinal Pigment Epithelium Butterfly-Shaped Pigment Dystrophy Early-Onset Nuclear Cataract Primary Open-Angle Glaucoma Type 1N Juvenile-Onset Primary Open-Angle Glaucoma Type 3 Juvenile-Onset Primary Open-Angle Glaucoma Type 2 Chandler Syndrome Thiel-Behnke Corneal Dystrophy Coloboma of Eyelid Colobomatous Microphthalmia Miller-Fisher Syndrome Optic Atrophy Type 2 Red Cell Aplasia Chronic Acquired Pure Red Cell Aplasia Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Congenital Dyserythropoietic Anemia Type 3 Southeast Asian Ovalocytosis Hereditary Pyropoikilocytosis Lymphomatoid Papulosis Lymphocyte-Rich Classical Hodgkin Lymphoma Aggressive Systemic Mastocytosis Atypical Chronic Myeloid Leukemia Acute Myeloid Leukemia with 11q23 Abnormalities Bilineal Acute Leukemia Primary Mediastinal Large B-Cell Lymphoma Familial Hypertrophic Cardiomyopathy Leber Hereditary Optic Neuropathy plus Disease Fried's Tooth and Nail Syndrome Metaphyseal Chondromatosis with D-2-Hydroxyglutaric Aciduria Dappled Diaphyseal Dysplasia Spondyloepimetaphyseal Dysplasia Type Handigodu Complete Androgen Insensitivity Syndrome Atlantoaxial Subluxation Fleck Retina of Kandori Acquired Von Willebrand Syndrome Multiple Ventricular Septal Defects Atrial Septal Defect Type Sinus venosus Atrial Septal Aneurysm Congenital Stenosis of the Inferior Vena Cava Aorto-Right Ventricular Tunnel Kommerell Diverticulum Persistent Fifth Aortic Arch Dysphagia Lusoria Cervical Aortic Arch Interventricular Septum Aneurysm Acquired Thrombotic Thrombocytopenic Purpura Autoinflammatory Syndrome Familial Thyroglossal Duct Cyst Neurofibromatosis Type 3 Humero-Ulnar Synostosis Neovascular Glaucoma Uremic Pruritus Brachydactyly Type A4 Brachydactyly Type C Brachydactyly Type B Brachydactyly Type B1 Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1 Bent Bone Dysplasia Acromesomelic Dysplasia Syndactyly Type 3 Neonatal Osteosclerotic Dysplasia Dense Deposit Disease Levocardia Mosaic Trisomy 8 Mosaic Trisomy 22 7q11.23 Duplication Syndrome Emanuel Syndrome Ring Chromosome 9 Ring Chromosome 11 Syndrome Pseudohypoparathyroidism Type 1B Pseudohypoparathyroidism Type 2 Hereditary Renal Hypouricemia Spinocerebellar Ataxia with Axonal Neuropathy Cerebellar Ataxia Type Cayman Angioma Serpiginosum Congenital Tracheomalacia Primary Progressive Aphasia Secondary Short Bowel Syndrome Congenital Disorder of Glycosylation Type 2H Congenital Malformation of the Tricuspid Valve Mesocardia Congenital Anomaly of Superior Vena Cava Anomalies of Great Veins, Congenital Atypical Arterial Duct Iatrogenic or Traumatic Pituitary Deficiency Acquired Premature Ovarian Failure Thyroid Dysgenesis Cytomegalic Congenital Adrenal Hypoplasia Congenital Non-Goitrous Hypothyroidism Type 3 Congenital Renal Artery Stenosis Infectious Disease of the Nervous System Fingerprint Body Myopathy Chronic Conjunctivitis Solar Urticaria Zebra Body Myopathy Reducing Body Myopathy 48,XXXY Syndrome Ring Chromosome 13 Ring Chromosome 15 Idiopathic Membranous Glomerulonephritis Sinding-Larsen-Johansson Disease Furlong Syndrome Carney-Stratakis Syndrome Familial Papillary Thyroid Carcinoma with Papillary Renal Cell Carcinoma Congenital Muscular Dystrophy Acute Myeloid Leukemia with Recurrent Genetic Anomaly Mastocytosis Indolent Systemic Mastocytosis Postinfectious Encephalitis Infectious Encephalitis 46,XY Disorder of Sex Development Familial Digital Arthropathy - Brachydactyly Infantile Osteopetrosis with Neuroaxonal Dysplasia Autosomal Recessive Osteopetrosis Type 5 Perineurioma Focal Segmental Glomerulosclerosis Type 4 Neurogenic Scapuloperoneal Syndrome Type Kaeser Hypochromic Microcytic Anaemia with Iron Overload Type 1 Fibronectin Glomerulopathy Hinman Syndrome Mycoplasma Encephalitis Congenital Primary Aphakia Microtia Florid Cemento-Osseous Dysplasia Immune Defect due to Absence of Thymus West Nile Virus Infection Desmoplastic Small Round Cell Tumor Pseudotyphus of California Punctate Palmoplantar Keratoderma Type 1 Ichthyosis Hystrix Gravior Ichthyosis Hystrix Type Curth-Macklin Nasal-Type Extranodal NK-T-Cell Lymphoma Hepatosplenic T-cell Lymphoma Enteropathy-Associated T-Cell Lymphoma Nodular Lymphocyte-Predominant Hodgkin Lymphoma Alpha-Heavy Chain Disease Gamma-Heavy Chain Disease T-Cell Prolymphocytic Leukemia Aggressive NK-Cell Leukemia Adult T-Cell Leukemia - Lymphoma Acute Myeloid Leukemia with Multilineage Dysplasia Acute Basophilic Leukemia Acute Biphenotypic Leukemia B-Cell Prolymphocytic Leukemia Chronic Neutrophilic Leukemia Unclassified Chronic Myeloproliferative Disease Juvenile Myelomonocytic Leukemia Refractory Anemia with Excess Blasts Acute Panmyelosis with Myelofibrosis AMME Syndrome Congenital Analbuminemia Aplasia of Lacrimal and Salivary Glands Congenital Malformation of Salivary Glands and Ducts Agenesis of Lacrimal and Salivary Glands Hereditary Amyloidosis with Primary Renal Involement Familial Amyloid Polyneuropathy Type 4 Juvenile Psoriatic Arthritis Systemic Juvenile Idiopathic Arthritis X-Linked Syndromic Mental Retardation Type Turner X-Linked Syndromic Mental Retardation Type 9 X-Linked Syndromic Mental Retardation Type 12 X-Linked Spinocerebellar Ataxia Type 4 X-Linked Syndromic Mental Retardation Type Stocco dos Santos X-Linked Syndromic Mental Retardation Type Siderius X-Linked Syndromic Intellectual Disability Type Schimke Wieacker-Wolff Syndrome MEHMO Syndrome Microphthalmia - Ankyloblepharon - Intellectual Disability Syndrome X-Linked Syndromic Mental Retardation Type 7 X-Linked Syndromic Intellectual Disability Type Abidi Genochondromatosis Type 1 Spondylo-Ocular Syndrome Idiopathic Juvenile Osteoporosis Metaphyseal Dysplasia Type Braun-Tinschert Autosomal Dominant Chondrodysplasia Punctata Chondrodysplasia punctata Type Toriello Tibial-Metacarpal Chondrodysplasia Punctata 3-Phosphoglycerate Dehydrogenase Deficiency Erythrokeratoderma Congenital Disorder of Glycosylation Type 1F Congenital Disorder of Glycosylation Type 1G Congenital Disorder of Glycosylation Type 1H Congenital Disorder of Glycosylation Type 1L Congenital Disorder of Glycosylation Type 2E Niemann-Pick Disease Type D Akesson Syndrome Oculocutaneous Albinism Type 3 Oculocutaneous Albinism Type 4 Cutaneous Mastocytoma Diffuse Cutaneous Mastocytosis X-Linked Lethal Multiple Pterygium Syndrome Pretibial Dystrophic Epidermolysis Bullosa Woolly Hair Nevus Skin Vascular Disease Subcutaneous Tissue Disease Chronic Nephritic Syndrome with Dense Deposit Disease Cryoglobulinemic Vasculitis Gonadotropic Pituitary Adenoma Cardiomyopathy - Hypotonia - Lactic Acidosis Syndrome Isolated Congenital Sclerocornea Congenital Ectropion Uveae Pilomatrixoma Familial Capillary Hemangioma Isolated Congenital Alacrima Ring Dermoid of Cornea Familial Congenital Palsy of Trochlear Nerve Early-Onset Anterior Polar Cataract Coralliform Cataract Cerulean Cataract Persistent Hyperplastic Primary Vitreous Snowflake Vitreoretinal Degeneration Congenital Esophageal Diverticulum Secondary Ciliary Dyskinesia Congenital Horner Syndrome Marcus-Gunn Syndrome Acquired Angioedema ACE Inhibitor-Induced Angioedema Isolated Cryptophthalmia Mitochondrial Non-Syndromic Sensorineural Deafness Deafness - Hypogonadism Syndrome Orofaciodigital Syndrome Type 7 Anonychia - Onychodystrophy Syndrome Telangiectasia Macularis Eruptiva Perstans Autosomal-Recessive Nonsyndromic Hearing Loss and Deafness DFNB61 Deafness, Autosomal Dominant 23 X-Linked Non-Syndromic Sensorineural Deafness Type DFN Disorder of Sex Development Brachyrachia Hypochondrogenesis Autosomal Recessive Spondyloepiphyseal Dysplasia Tarda Polysyndactyly Polydactyly of a Biphalangeal Thumb Postaxial Polydactyly Type A4 Renal Dysplasia, Bilateral Pauci-Immune Glomerulonephritis Renal Cysts and Diabetes Syndrome Posterior Urethral Valve Unilateral Renal Hypoplasia Thanatophoric Dysplasia Type Glasgow Short Rib-Polydactyly Syndrome, Verma-Naumoff Type Crouzon Syndrome-Acanthosis Nigricans Syndrome Fragile X-Associated Tremor - Ataxia Syndrome Severe Infantile Polycystic Kidney Disease with Tuberous Sclerosis Langerhans Cell Sarcoma Follicular Dendritic Cell Sarcoma Dendritic Cell Sarcoma Not Otherwise Specified Idiopathic Hemiconvulsion-Hemiplegia Syndrome Myoclonic Epilepsy of Infancy Lymphedema - Cerebral Arteriovenous Anomaly Syndrome Sialidosis Type 2 Autosomal Recessive Mental Retardation Type 34 Autosomal Recessive Mental Retardation Type 28 Autosomal Recessive Mental Retardation Type 25 Autosomal Recessive Mental Retardation Type 24 Autosomal Recessive Mental Retardation Type 23 Autosomal Recessive Mental Retardation Type 19 Autosomal Recessive Mental Retardation Type 30 Autosomal Recessive Mental Retardation Type 33 Autosomal Recessive Mental Retardation Type 29 Autosomal Recessive Mental Retardation Type 18 Autosomal Recessive Mental Retardation Type 16 Autosomal Recessive Mental Retardation Type 14 Autosomal Recessive Mental Retardation Type 4 Autosomal Recessive Mental Retardation Type 11 Autosomal Recessive Mental Retardation Type 10 Autosomal Recessive Mental Retardation Type 9 Autosomal Recessive Mental Retardation Type 7 Autosomal Recessive Mental Retardation Type 6 Autosomal Recessive Mental Retardation Type 12 Autosomal Recessive Mental Retardation Type 1 Familial Acute Necrotizing Encephalopathy Isolated Congenital Anosmia Tritanopia Ichthyosis-Prematurity Syndrome Superior Limbic Keratoconjunctivitis Familial Anterior Segment Mesenchymal Dysgenesis Hypomyelinating Leukodystrophy Type 8 Amelogenesis Imperfecta Amelogenesis Imperfecta Type 1H Amelogenesis Imperfecta Type 2A4 X-Linked Amelogenesis Imperfecta Type 2 Amelogenesis Imperfecta Type 2A1 Amelogenesis Imperfecta Type 3A Amelogenesis Imperfecta Type 4 Charcot-Marie-Tooth Disease - Deafness - Intellectual Disability Invasive Infections due to Vancomycin-Resistant Enterococci Scarring in Glaucoma Filtration Surgical Procedures Autosomal Recessive Cutis Laxa Type 2 Autosomal Recessive Cutis Laxa Type 1 Xeroderma Pigmentosum Variant Early-Onset Sarcoidosis Warm Autoimmune Hemolytic Anemia IgG4-Related Hepatopathy Radiation Myelitis Guam Disease Deafness with Labyrinthine Aplasia - Microtia - Microdontia Moderate and Severe Traumatic Brain Injury Moderate and Severe Traumatic Cerebral Edema Hematopoietic Stem Cell Transplantation Acute Sensorineural Hearing Loss by Acute Acoustic Trauma Familial Pseudohyperkalemia Bacterial Sepsis of Newborn Sepsis of Newborn due to Other and Unspecified Streptococci Sepsis in Premature Infants Partial Deep Dermal and Full Thickness Burns Mitochondrial Disease Peroxisomal Disease Rare Inborn Errors of Metabolism Hereditary Persistence of Fetal Hemoglobin Bullous Systemic Lupus Erythematosus Cerebral Arteriovenous Malformation Papillary Renal Cell Carcinoma Type 1 Idiopathic Neonatal Atrial Flutter Incessant Infant Ventricular Tachycardia Miyoshi Myopathy Type 2 PHACE Syndrome Generalized Arterial Calcification of Infancy Kikuchi-Fujimoto Disease Keratolytic Winter Erythema Familial Short QT Syndrome Torsade-De-Pointes Syndrome with Short Coupling Interval Mesothelioma Malignant Mesothelioma Primary Effusion Lymphoma Lissencephaly Achromatopsia Type 4 IgG4-Related Retroperitoneal Fibrosis Cornea Plana Type 2 Cornea Plana Type 1 Lethal Arthrogryposis - Anterior Horn Cell Disease Syndrome Cobb Syndrome Distal Spinal Muscular Atrophy Thrombotic Microangiopathy Posterior Cortical Atrophy Left Ventricular Noncompaction Hereditary Geniospasm Goldmann-Favre Syndrome Congenital Lactase Deficiency Isolated Follicle Stimulating Hormone Deficiency Systemic Vasculitis Familial Cutaneous Collagenoma MALT Lymphoma Inclusion Body Myopathy - Paget Disease - Frontotemporal Dementia Type 3 Inclusion Body Myopathy - Paget Disease - Frontotemporal Dementia Type 2 Corneal Dystrophies Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia Severe Idiopathic Pneumococcemia Idiopathic Disseminated Cytomegalovirus Infection Idiopathic Recurrent and Disabling Cutaneous Herpes Granulomatous Slack Skin Medullary Cystic Kidney Disease Type 2 Combined Deficiency of Factors V - VIII Type 2 Combined Deficiency of Factors V - VIII with Normal Protein C and Protein C Inhibitor Combined Deficiency of Factors V - VIII Familial Vascular Leukoencephalopathy Paraneoplastic Neurologic Syndrome Congenital Sucrase-Isomaltase Deficiency Epidermal Nevus Syndrome Isolated Synostotic Plagiocephaly Mitochondrial DNA Depletion Syndrome Madelung Deformity Coloboma of Optic Papilla Iminoglycinuria Bietti Crystalline Dystrophy Parasomnia Autoimmune Hypoparathyroidism Chronic Interstitial Cystitis Uveal Melanoma Acute graft versus host disease Müllerian Aplasia Retinal Dystrophy Psychogenic Movement Disorders Proopiomelanocortin Deficiency Cancer-Associated Retinopathy Familial Isolated Restrictive Cardiomyopathy Osteosclerosis-Ichthyosis-Premature Ovarian Failure Syndrome Central Neurocytoma Intestinal Lymphangiectasia Oguchi Disease Type 2 Cystoid Macular Dystrophy Familial Drusen Progressive Bifocal Chorioretinal Atrophy North Carolina Macular Dystrophy Inclusion Body Myopathy Type 3 Majeed Syndrome Syndromic Microphthalmia Type 10 Respiratory Bronchiolitis Interstitial Lung Disease Acute Interstitial Pneumonia Hepatic Veno-Occlusive Disease-Immunodeficiency Syndrome Bickerstaff Brainstem Encephalitis Grange Syndrome Atrophodermia Vermiculata