Viral Infectious Disease,Chronic Cholangitis,Cholangitis,Autoimmune Cholangitis,Primary Biliary Cholangitis,Herpes Simplex,Cholangitis, Primary Sclerosing,Acute Promyelocytic Leukemia,Autoimmune Disease Of Gastrointestinal Tract,Crest Syndrome,Bjornstad Syndrome

Seizure Disorder,Alzheimer Disease,Non-Specific Syndromic Intellectual Disability,17q24.2 Microdeletion Syndrome,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Neurodevelopmental Disorder With Dysmorphic Facies And Distal Limb Anomalies,Disease Of Mental Health,Legius Syndrome,Autism

Hepatocellular Carcinoma,Glycogen Storage Disease Iv

Dissociative Disorder,Culler-Jones Syndrome

Acinar Cell Cystadenocarcinoma

Muscular Disease,Chronic Myelomonocytic Leukemia,Muscle Tissue Disease,Orbital Plasma Cell Granuloma,Antisynthetase Syndrome,Myositis,Differentiated Thyroid Carcinoma,Chronic Orbital Inflammation,Adult Dermatomyositis,Childhood Type Dermatomyositis

Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome,Breast Cancer,Colorectal Cancer,Oligospermia,Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant,Retinoblastoma,Neuropathy, Hereditary Sensory, Type Ie,Oculoauricular Syndrome,Cartilage-Hair Hypoplasia

Lateral Meningocele Syndrome

Skin Melanoma,Melanoma,Breast Cancer,Mental Retardation, Autosomal Recessive 65,Retinoblastoma,Autism Spectrum Disorder,Autosomal Dominant Non-Syndromic Intellectual Disability,Autosomal Recessive Non-Syndromic Intellectual Disability,Autism

Atrophy Of Testis,Ohdo Syndrome, Sbbys Variant,Kleefstra Syndrome 1,Ohdo Syndrome

Desmoid Disease, Hereditary

Leukemia, Acute Myeloid,Acute Megakaryoblastic Leukemia Without Down Syndrome,Acute Megakaryocytic Leukemia,Meier-Gorlin Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Retinoblastoma,Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type,Childhood Acute Myeloid Leukemia

Epilepsy,Non-Specific Syndromic Intellectual Disability,Kleefstra Syndrome 2,Disease Of Mental Health,O'Donnell-Luria-Rodan Syndrome,Cerebroretinal Microangiopathy With Calcifications And Cysts 1,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Autism

Hepatic Veno-Occlusive Disease,Crohn'S Disease,Multiple Sclerosis,Hepatic Venoocclusive Disease With Immunodeficiency,Acute Promyelocytic Leukemia

Tuberculum Sellae Meningioma,Griscelli Syndrome, Type 3,Ohdo Syndrome, Sbbys Variant,Sella Turcica Neoplasm,Schizophrenia,Ohdo Syndrome

Ovarian Cancer,Pick Disease Of Brain,Chromosome 1p36 Deletion Syndrome,Ovarian Cancer 1

Cleft Lip,Cleft Lip/Palate,X-Linked Intellectual Disability, Siderius Type,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Van Der Woude Syndrome 1,Disease Of Mental Health,Orofacial Cleft,Non-Syndromic X-Linked Intellectual Disability,Borjeson-Forssman-Lehmann Syndrome,Acute Promyelocytic Leukemia,Kabuki Syndrome 1,Syndromic X-Linked Intellectual Disability,Autism,Syndromic X-Linked Intellectual Disability Siderius Type

Flying Phobia,Chromosomal Disease,Uterine Carcinosarcoma,Charge Syndrome,Squamous Cell Carcinoma,Retinitis Pigmentosa,Cornelia De Lange Syndrome,Cockayne Syndrome A,T-Cell Lymphoblastic Leukemia/Lymphoma,Amelogenesis Imperfecta,Rare Genetic Intellectual Disability,Menke-Hennekam Syndrome,Leukemia, Acute Myeloid,Familial Isolated Hypoparathyroidism,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Human T-Cell Leukemia Virus Type 1,Human T-Cell Leukemia Virus Type 2,Monocytic Leukemia,Cockayne Syndrome,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Microphthalmia,Colorectal Cancer,Microcephaly,Hypoxia,Polydactyly, Postaxial, Type A1,Alacrima, Achalasia, And Mental Retardation Syndrome,Sarcoma,Fibrosarcoma,Prostate Cancer,Disease Of Mental Health,Rubinstein-Taybi Syndrome 2,Cervical Cancer,Chromosome 3pter-P25 Deletion Syndrome,Chromosome 16p13.3 Deletion Syndrome, Proximal,Retinoblastoma,Type 2 Diabetes Mellitus,Rubinstein-Taybi Syndrome 1,Lynch Syndrome,Lung Squamous Cell Carcinoma,Albinism, Ocular, With Late-Onset Sensorineural Deafness,Bladder Urothelial Carcinoma,Neural Tube Defects,Menke-Hennekam Syndrome 2,Esophageal Cancer,Thumb Deformity,Early Infantile Epileptic Encephalopathy,Diffuse Large B-Cell Lymphoma,Gastrointestinal Stromal Tumor,Holt-Oram Syndrome,Huntington Disease,Congenital Disorder Of Glycosylation, Type Ig,Kabuki Syndrome 1,Leukemia, Acute Monocytic,Amelogenesis Imperfecta, Type Ig,Autosomal Dominant Non-Syndromic Intellectual Disability,Otopalatodigital Syndrome, Type I,Hennekam Syndrome,Chromosomal Deletion Syndrome,Nut Midline Carcinoma,Medulloblastoma,Leigh Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability 19,Lung Cancer,Pancreatic Cancer

Charge Syndrome,Plasma Cell Neoplasm,Cold Agglutinin Disease,Kleefstra Syndrome,Cavernous Sinus Meningioma,Rasopathy,Holoprosencephaly,Hypoplastic Left Heart Syndrome,Leukemia, Acute Myeloid,Dandy-Walker Syndrome,Rubinstein Taybi Like Syndrome,Breast Malignant Phyllodes Tumor,Microphthalmia,Microcephaly,Weaver Syndrome,Sotos Syndrome 1,Alacrima, Achalasia, And Mental Retardation Syndrome,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Complement Component C1s Deficiency,Chromosome 16p13.3 Deletion Syndrome, Proximal,Mental Retardation, Autosomal Dominant 26,Childhood Medulloblastoma,Lung Squamous Cell Carcinoma,Smith-Magenis Syndrome,Spinocerebellar Ataxia 2,Tetralogy Of Fallot,Peripheral T-Cell Lymphoma,Congenital Disorder Of Glycosylation, Type Ig,Autism Spectrum Disorder,Lymphoma,Kabuki Syndrome 1,Kbg Syndrome,Methylmalonic Acidemia And Homocysteinemia, Cblx Type,Scoliosis,Autosomal Dominant Non-Syndromic Intellectual Disability,Myeloma, Multiple,Medulloblastoma,Isolated Growth Hormone Deficiency Type Iii,Postaxial Acrofacial Dysostosis

Childhood Acute Lymphocytic Leukemia,Lymphoblastic Lymphoma,Hypertrichosis,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Cornelia De Lange Syndrome,Leukemia, Chronic Myeloid,Acute Myeloid Leukemia With T(9;11)(P22;Q23),B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Rare Genetic Intellectual Disability,Myeloproliferative Neoplasm,Leukemia,Pancytopenia,Mixed Phenotype Acute Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With 11q23 Abnormalities,Intravascular Large B-Cell Lymphoma,Familial Isolated Trichomegaly,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Ring Chromosome 21,Acute Megakaryoblastic Leukemia Without Down Syndrome,Rubinstein Taybi Like Syndrome,Central Nervous System Leukemia,Monocytic Leukemia,Ring Chromosome,Myeloid Sarcoma,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Acute Monoblastic Leukemia,Colon Leiomyoma,Cytogenetically Normal Acute Myeloid Leukemia,Microcephaly,Hypoxia,Chronic Granulomatous Disease,Alacrima, Achalasia, And Mental Retardation Syndrome,Leukemia, Acute Lymphoblastic 3,Disease Of Mental Health,Cornelia De Lange Syndrome 1,Lymphoma, Non-Hodgkin, Familial,Wiedemann-Steiner Syndrome,Myelodysplastic Syndrome,Hairy Elbows,Acute Promyelocytic Leukemia,Wilms Tumor 1,Kabuki Syndrome 1,Kbg Syndrome,Leukemia, Acute Monocytic,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism

Epilepsy,Potocki-Shaffer Syndrome,Kleefstra Syndrome,Meier-Gorlin Syndrome 1,Weaver Syndrome,Syndromic Intellectual Disability,Intellectual Developmental Disorder With Behavioral Abnormalities And Craniofacial Dysmorphism With Or Without Seizures,Autism Spectrum Disorder,Kabuki Syndrome 1,Kbg Syndrome,Parietal Foramina,Autism

Kleefstra Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Kabuki Syndrome 1

Plasma Cell Neoplasm,Kleefstra Syndrome,Leukemia,Leukemia, Acute Myeloid,Kleefstra Syndrome Due To A Point Mutation,Cystic Kidney Disease,Colorectal Cancer,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Kleefstra Syndrome 2,Disease Of Mental Health,Kleefstra Syndrome 1,Autism Spectrum Disorder,Kabuki Syndrome 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Nut Midline Carcinoma,Myeloma, Multiple,Cardiomyopathy, Infantile Histiocytoid

Xeroderma Pigmentosum, Variant Type