Barrett'S Adenocarcinoma,Hepatocellular Carcinoma,Type 1 Diabetes Mellitus 3

Adenosquamous Gallbladder Carcinoma

Hemochromatosis Type 2

Legionellosis

Acetaminophen Metabolism,Endometrial Cancer,Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Macular Telangiectasia Type 2,Liver Benign Neoplasm,Suppression Of Tumorigenicity 12,Gastroesophageal Adenocarcinoma,Diabetes Mellitus,Alzheimer Disease,Diffuse Gastric Cancer,Oral Mucosa Leukoplakia,Occupational Asthma,Intracranial Meningioma,Multiple Chemical Sensitivity,Motor Neuron Disease,Substance Dependence,Alcoholic Pancreatitis,Leukemia, Acute Lymphoblastic,Liver Cirrhosis,Larynx Cancer,Papilloma,Ovarian Cyst,Kidney Cancer,Transitional Cell Carcinoma,Bladder Cancer,Hellp Syndrome,Asbestosis,Aplastic Anemia,Ovarian Cancer,Cardia Cancer,Testicular Cancer,Charcot-Marie-Tooth Disease,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Hepatocellular Carcinoma,Tooth Disease,Polyneuropathy Due To Drug,Oligospermia,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Exfoliation Syndrome,Type 2 Diabetes Mellitus,Lynch Syndrome,Familial Adenomatous Polyposis,Kala-Azar 2,Esophageal Cancer,Barrett Esophagus,Myelodysplastic Syndrome,Deafness, X-Linked 7,Tobacco Addiction,Colorectal Adenoma,Hepatocellular Adenoma,Pulmonary Disease, Chronic Obstructive,Renal Cell Carcinoma, Nonpapillary,Autism Spectrum Disorder,Oligoasthenoteratozoospermia,Lung Cancer,Asthma

Retinitis Pigmentosa,Intermediate Malignant Teratoma,Filarial Elephantiasis,Noonan Syndrome 1,Skin Papilloma,Breast Fibrosarcoma,Polyneuropathy Due To Drug,Pseudopterygium,Cone-Rod Dystrophy 2,Disease Of Mental Health,Inflammatory Bowel Disease 16,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Hypertension, Essential

Hepatocellular Carcinoma

Mixed Phenotype Acute Leukemia,Hepatocellular Carcinoma

Robinow Syndrome, Autosomal Recessive 1,Leukodystrophy,Parkinson Disease, Late-Onset,Microcephaly,Leukodystrophy, Hypomyelinating, 17,Lynch Syndrome,Developmental And Epileptic Encephalopathy 29,Robinow Syndrome,Lung Cancer,Leukodystrophy, Hypomyelinating, 3

Tyrosinemia,Barrett'S Adenocarcinoma,Tyrosinemia, Type I,Maleylacetoacetate Isomerase Deficiency,Lactic Acidosis,Alkaptonuria,Pyruvate Dehydrogenase E1-Alpha Deficiency

Colorectal Cancer,Gallbladder Cancer

Exudative Vitreoretinopathy 2, X-Linked

Gastroesophageal Adenocarcinoma,Diffuse Gastric Cancer,Beta-Thalassemia Major,Oral Cancer,Oral Leukoplakia,Isolated Cleft Lip,Senile Cataract,Motor Neuron Disease,Basal Cell Carcinoma,Larynx Cancer,Bladder Cancer,Thyroid Tumor,Asbestosis,Leukoplakia,Aplastic Anemia,Cardia Cancer,Oligospermia,Toxic Encephalopathy,Mutagen Sensitivity,Lynch Syndrome,Sister Chromatid Exchange, Frequency Of,Orofacial Cleft,Myelodysplastic Syndrome

Alzheimer Disease,Parkinson Disease, Late-Onset,Hepatocellular Carcinoma,Night Blindness, Congenital Stationary, Type 1a

Xq28 Duplication Syndrome, Int22h1/Int22h2 Mediated,Murray Valley Encephalitis,Variegate Porphyria,Developmental And Epileptic Encephalopathy 8,Chromosome Xq28 Duplication Syndrome,Mental Retardation, X-Linked, Syndromic 32,Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency,Non-Syndromic X-Linked Intellectual Disability,Syndromic X-Linked Intellectual Disability Snyder Type

Mitochondrial Encephalomyopathy,Muscular Disease,X-Linked Recessive Disease,Chromosomal Disease,Physical Disorder,Glucose Metabolism Disease,Retinitis Pigmentosa,Myopathy,Amino Acid Metabolic Disorder,Connective Tissue Disease,Disorder Of Sexual Development,Robinow Syndrome, Autosomal Recessive 1,Inherited Metabolic Disorder,Muscle Tissue Disease,Charcot-Marie-Tooth Disease, Dominant Intermediate C,Neuromuscular Disease,Mitochondrial Myopathy,Mitochondrial Metabolism Disease,Infantile Liver Failure Syndrome,Antisynthetase Syndrome,Amyotrophic Lateral Sclerosis 1,Combined Oxidative Phosphorylation Deficiency 12,Angelman Syndrome,Eye Degenerative Disease,Microcephaly-Short Stature-Intellectual Disability-Facial Dysmorphism Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2d,Motor Neuron Disease,Subependymal Glioma,Benign Ependymoma,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Epilepsy, Idiopathic Generalized 3,Congenital Nervous System Abnormality,Subependymal Giant Cell Astrocytoma,Cardiovascular System Disease,Auditory System Disease,Lung Disease,Acute Cystitis,Parasitic Protozoa Infectious Disease,Trichohepatoenteric Syndrome 1,Pleurisy,Immune System Disease,Nervous System Disease,Inner Ear Disease,Leukodystrophy,Eye Disease,Charcot-Marie-Tooth Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2n,Early Myoclonic Encephalopathy,Peripheral Nervous System Disease,Microcephaly,Dysphagia,Central Nervous System Disease,Cerebral Degeneration,46 Xx Gonadal Dysgenesis,West Syndrome,Disease Of Mental Health,Leukodystrophy, Hypomyelinating, 15,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Respiratory System Disease,Microcephaly, Progressive, With Seizures And Cerebral And Cerebellar Atrophy,Integumentary System Disease,Polyomavirus-Associated Nephropathy,Disease By Infectious Agent,Deafness, Autosomal Recessive 89,Sensory System Disease,Usher Syndrome,Lennox-Gastaut Syndrome,Immune Deficiency Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2u,Neonatal Period Electroclinical Syndrome,Early Infantile Epileptic Encephalopathy,X-Linked Monogenic Disease,Autosomal Recessive Disease,Autosomal Genetic Disease,Perrault Syndrome,Hemorrhagic Cystitis,Pulmonary Disease, Chronic Obstructive,Usher Syndrome, Type Iiib,Epilepsy, Idiopathic Generalized 2,Specific Developmental Disorder,Pervasive Developmental Disorder,Acquired Metabolic Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Robinow Syndrome,Pontocerebellar Hypoplasia,Chromosome 16p11.2 Deletion Syndrome,Chromosomal Duplication Syndrome,Hypomyelinating Leukodystrophy,Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes,Thrombosis,Neuronopathy, Distal Hereditary Motor, Type Va

Robinow Syndrome, Autosomal Recessive 1,Developmental And Epileptic Encephalopathy 29,Robinow Syndrome