Colon Small Cell Carcinoma,Pineal Region Germinoma,B-Cell Adult Acute Lymphocytic Leukemia

Diamond-Blackfan Anemia 4,Premature Menopause,Disease Of Mental Health,Scalp-Ear-Nipple Syndrome,Fragile X Syndrome

Endometrial Stromal Sarcoma,Myopathy,Myotonic Disease,Amyotrophic Lateral Sclerosis 1,Myotonic Dystrophy 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Atrial Septal Defect 1,Agammaglobulinemia,Endometrial Stromal Tumor,Myotonic Dystrophy 2,Congenital Myasthenic Syndrome,Dermatopathia Pigmentosa Reticularis,Mental Retardation, X-Linked, Syndromic, Bain Type,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism,Syndromic X-Linked Intellectual Disability 94

Porokeratosis

Fissured Tongue,Amyotrophic Lateral Sclerosis 11,Yunis-Varon Syndrome,Atypical Juvenile Parkinsonism,Amyotrophic Lateral Sclerosis 1,Undetermined Early-Onset Epileptic Encephalopathy,Foramen Magnum Meningioma,Developmental And Epileptic Encephalopathy 53,Dystonia,Charcot-Marie-Tooth Disease,Parkinson Disease, Late-Onset,Ciliary Dyskinesia, Primary, 26,Bipolar Disorder,Parkinson Disease 20, Early-Onset,West Syndrome,Disease Of Mental Health,Charcot-Marie-Tooth Disease, Type 4j,Down Syndrome,Parkinson Disease 21,Developmental And Epileptic Encephalopathy 1,Lowe Oculocerebrorenal Syndrome,Chromosomal Duplication Syndrome,Parkinson Disease 2, Autosomal Recessive Juvenile,Joubert Syndrome 1

Connective Tissue Disease,Autoimmune Disease,Neuropathy, Hereditary Sensory And Autonomic, Type Iib,Mixed Connective Tissue Disease,Syndromic Intellectual Disability,Neuropathy, Hereditary Sensory And Autonomic, Type Iia

Endometrial Stromal Sarcoma,Myopathy,Congenital Lymphedema,Myotonic Disease,Myotonic Dystrophy 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Spinocerebellar Ataxia 8,Atrial Septal Defect 1,Endometrial Stromal Tumor,Precursor T-Cell Acute Lymphoblastic Leukemia,Myotonic Dystrophy 2,Congenital Myasthenic Syndrome,Dermatopathia Pigmentosa Reticularis,Hereditary Lymphedema,Mental Retardation, X-Linked, Syndromic, Bain Type

Gastrointestinal Neuroendocrine Benign Tumor,Spleen Cancer,Gastric Neuroendocrine Neoplasm,Breast Liposarcoma,Wolfram Syndrome 2,Mullegama-Klein-Martinez Syndrome,Chromosome 1p36 Deletion Syndrome

Immunodeficiency With Hyper-Igm, Type 2

Amyotrophic Lateral Sclerosis 1

Frontotemporal Dementia

Narcolepsy

Cancer-Associated Retinopathy,Patellar Tendinitis

Lung Acinar Adenocarcinoma

Hepatocellular Carcinoma

Med23,Alazami Syndrome,Disease Of Mental Health,Coffin-Siris Syndrome 9,Kbg Syndrome,Isolated Growth Hormone Deficiency,Isolated Growth Hormone Deficiency, Type Ia

Systemic Lupus Erythematosus

Diffuse Glomerulonephritis,Epidermolysis Bullosa, Junctional, Herlitz Type,Hemolytic Uremic Syndrome, Atypical 1,Coffin-Siris Syndrome 1,Arthrogryposis Multiplex Congenita 2, Neurogenic Type

Connective Tissue Disease,Parainfluenza Virus Type 3,Sjogren Syndrome,Growth Hormone Deficiency,Mixed Connective Tissue Disease,Limited Scleroderma,Isolated Growth Hormone Deficiency, Type V,Systemic Lupus Erythematosus,Isolated Growth Hormone Deficiency,Microcephalic Osteodysplastic Primordial Dwarfism, Type I,Isolated Growth Hormone Deficiency, Type Ia

Hypertropia,Leukodystrophy,Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant

Fibrogenesis Imperfecta Ossium,Greenberg Dysplasia,Melorheostosis,Melorheostosis With Osteopoikilosis,Emery-Dreifuss Muscular Dystrophy,Osteopoikilosis,Acute Inflammation Of Lacrimal Passage,Dacryocystitis,Elastoma,Arteriovenous Malformations Of The Brain,Congenital Muscular Dystrophy-Dystroglycanopathy A7,Axial Osteomalacia,Vertebrobasilar Insufficiency,12q14 Microdeletion Syndrome,Buschke-Ollendorff Syndrome,Muscular Dystrophy, Congenital, Lmna-Related,Pelger-Huet Anomaly,Ornithosis,Hutchinson-Gilford Progeria Syndrome,Cardiomyopathy, Dilated, 1h,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Odontochondrodysplasia,Walker-Warburg Syndrome,Congenital Disorder Of Glycosylation, Type In,Endosteal Hyperostosis, Autosomal Dominant,Emery-Dreifuss Muscular Dystrophy 1, X-Linked

Variola Minor,Cone-Rod Dystrophy 2,Hemolytic Uremic Syndrome, Atypical 1

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome

Motor Neuron Disease,Rift Valley Fever,Waardenburg Syndrome, Type 4b,Myotonic Dystrophy 2,Waardenburg Syndrome, Type 4a,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Dengue Virus

Neuromuscular Disease,Myotonic Disease,Myotonic Dystrophy 1,Neurofibromatosis, Type I,Muscular Dystrophy,Myotonic Dystrophy,Spinocerebellar Ataxia 8,Oculopharyngeal Muscular Dystrophy,Myotonic Dystrophy 2,Lens Disease,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Fragile X Syndrome,Huntington Disease-Like 2,Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Spinal And Bulbar Muscular Atrophy, X-Linked 1

Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Syndromic X-Linked Intellectual Disability,Syndromic X-Linked Intellectual Disability Shashi Type

Combined D-2- And L-2-Hydroxyglutaric Aciduria,Ivic Syndrome,Ischiocoxopodopatellar Syndrome With Or Without Pulmonary Arterial Hypertension

Ulcerative Blepharitis,Spinal Muscular Atrophy,Salpingitis Isthmica Nodosa

Diabetes Mellitus,Wolfram Syndrome 1,Testicular Cancer,Wolfram Syndrome,Hepatocellular Carcinoma,Type 2 Diabetes Mellitus,Maturity-Onset Diabetes Of The Young

Acth-Secreting Pituitary Adenoma,Cryptorchidism, Unilateral Or Bilateral

Neurodevelopmental Disorder With Speech Impairment And Dysmorphic Facies,Epilepsy,Nasal Cavity Benign Neoplasm,Myopathy, Centronuclear, 1,Malt Worker'S Lung,Prostate Squamous Cell Carcinoma,Primary Hyperoxaluria,Microcephaly,Kleefstra Syndrome 2,Disease Of Mental Health,Schizophrenia,Epilepsy, Early-Onset, With Or Without Developmental Delay,Kabuki Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 1

Articulation Disorder,Speech Disorder,Mucolipidosis,Tibial Neuropathy,Dyslexia,Tarsal Tunnel Syndrome,Vestibulocochlear Nerve Disease,Vestibular Neuronitis,Osteochondrosis,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Gnptab-Related Disorders,Gm2-Gangliosidosis, Ab Variant,Gingival Hypertrophy,Disseminated Chorioretinitis,Benign Essential Hypertension,Mucolipidoses,Deficiency Anemia,46,Xy Sex Reversal 7,Osteogenesis Imperfecta, Type Vii,Scheuermann Disease,Autosomal Recessive Disease,Hurler Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2v,Her2-Receptor Positive Breast Cancer,Stuttering,Legg-Calve-Perthes Disease,Mucolipidosis Ii Alpha/Beta,Mucolipidosis Iii Alpha/Beta,Mucolipidosis Iii Gamma,Mucopolysaccharidosis, Type Iiia

Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Myopathy,Connective Tissue Disease,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Muscular Atrophy,Bagassosis,Endometrial Stromal Tumor,Oculopharyngeal Muscular Dystrophy,Multisystem Proteinopathy,Disease Of Mental Health,Mixed Connective Tissue Disease,Fragile X-Associated Tremor/Ataxia Syndrome,Atrial Septal Defect 2

Mouth Disease

Retinitis Pigmentosa,Myotonic Dystrophy 1,Paraneoplastic Neurologic Disorders,Pontocerebellar Hypoplasia, Type 7,Spinal Muscular Atrophy,Motor Neuron Disease,Muscular Atrophy,Neuroblastoma,Sensory Peripheral Neuropathy,Hallucinogen Abuse,Atrial Septal Defect 1,Cone-Rod Dystrophy 6,Parkinson Disease, Late-Onset,Hyperinsulinemic Hypoglycemia, Familial, 4,Disease Of Mental Health,Retinitis Pigmentosa 49,Scalp-Ear-Nipple Syndrome,Fragile X Syndrome,Lambert-Eaton Myasthenic Syndrome,Lung Cancer

Viral Exanthem,Erythema Infectiosum,Lung Cancer

Spinal Muscular Atrophy

Robinow Syndrome, Autosomal Dominant 1,Robinow Syndrome

Chromophobe Renal Cell Carcinoma,Cleft Palate, Isolated,Deafness, Autosomal Recessive 109

Primary Optic Atrophy,Heinz Body Anemias

Kidney Hypertrophy,Atrial Septal Defect 1,Myotonic Dystrophy 2

Pontocerebellar Hypoplasia

Brain Compression

Amyotrophic Lateral Sclerosis 1,Feingold Syndrome 1,Intestinal Atresia,Pancreas, Annular,Vacterl Association,Gastrointestinal Defects And Immunodeficiency Syndrome,Pallister-Hall Syndrome,Microphthalmia, Syndromic 3,Anus, Imperforate

Sarcoma,Dermatopathia Pigmentosa Reticularis,Systemic Lupus Erythematosus

Lattice Corneal Dystrophy,Myopathy,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Muscular Dystrophy,Bagassosis,Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 3,Oculopharyngeal Muscular Dystrophy,Multisystem Proteinopathy,Dementia,Paget'S Disease Of Bone,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 2,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Fragile X Syndrome,Spinocerebellar Ataxia 2,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,X-Linked Hereditary Ataxia,Epithelial-Stromal Tgfbi Dystrophy,Lung Cancer,Frontotemporal Dementia

Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Spinocerebellar Ataxia 1,Frontotemporal Dementia

Infertility,Azoospermia

Metaphyseal Chondrodysplasia, Schmid Type,X-Linked Intellectual Disability With Marfanoid Habitus,Pancreatic Adenosquamous Carcinoma,Microcephaly,Disease Of Mental Health,Fryns Syndrome,Spermatogenic Failure 24,Non-Syndromic X-Linked Intellectual Disability,Opitz-Kaveggia Syndrome,Autism

Noonan Syndrome 7,Mouth Disease

Heart Disease,Small Intestine Neuroendocrine Neoplasm,Small Intestine Benign Neoplasm,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Xp11-Associated,Mental Retardation, X-Linked, Syndromic 34,Syndromic Intellectual Disability

Autoimmune Disease,Atrial Septal Defect 2

Familial Febrile Seizures,Atrial Septal Defect 1,Specific Language Impairment

Spinal Muscular Atrophy,Bladder Clear Cell Adenocarcinoma,Contagious Pustular Dermatitis,Laryngotracheitis

Psychotic Disorder,Schizoaffective Disorder,Schizophrenia 19,Schizophrenia

Malignant Exocrine Pancreas Neoplasm,Atrial Heart Septal Defect,Skin Angiosarcoma,Colorectal Cancer,Microcephaly,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Renal Cell Carcinoma, Papillary, 1,Tarp Syndrome,Microcephalic Osteodysplastic Primordial Dwarfism, Type I

Diamond-Blackfan Anemia,Ulnar-Mammary Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Autosomal Dominant Non-Syndromic Intellectual Disability 1

Acute Promyelocytic Leukemia,Carnitine-Acylcarnitine Translocase Deficiency

Childhood Absence Epilepsy,Ischemic Neuropathy,Myotonic Disease,Myotonic Dystrophy 1,Neuroblastoma,Spinal And Bulbar Muscular Atrophy, X-Linked 1

Hepatitis D,Leukemia, Acute Myeloid,Diamond-Blackfan Anemia,Cockayne Syndrome,Macular Degeneration, Age-Related, 1,Dermatopathia Pigmentosa Reticularis

Fanconi Anemia, Complementation Group A

Intellectual Developmental Disorder, Autosomal Recessive 71,Non-Syndromic X-Linked Intellectual Disability,Autosomal Recessive Non-Syndromic Intellectual Disability

Down Syndrome

Breast Adenomyoepithelioma,Large Cell Acanthoma,Pilar Sheath Acanthoma,Breast Myoepithelial Neoplasm,Angioma Serpiginosum,Desmoid Disease, Hereditary

Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Extraosseous Ewing Sarcoma,Clear Cell Sarcoma,Spindle Cell Sarcoma,Chondrosarcoma,Rhabdomyosarcoma 2,Sarcomatoid Basal Cell Carcinoma,Malignant Fibrous Histiocytoma,Melanoma,Rare Tumor,Cerebellar Angioblastoma,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Bladder Sarcoma,Melanoma Of Soft Tissue,Bone Epithelioid Hemangioma,Fibrous Histiocytoma,Peripheral Nervous System Neoplasm,Connective Tissue Cancer,Bone Sarcoma,Desmoplastic Small Round Cell Tumor,Constipation,Vulvar Sarcoma,Mucoepidermoid Carcinoma,Extraskeletal Mesenchymal Chondrosarcoma,Extraosseous Chondrosarcoma,Atypical Teratoid Rhabdoid Tumor,Astroblastoma,Intracranial Primitive Neuroectodermal Tumor,Neurofibromatosis, Type I,Sarcomatosis,Neuroblastoma,Myoepithelial Carcinoma,Cauda Equina Neoplasm,Childhood Malignant Schwannoma,Kidney Clear Cell Sarcoma,Middle Ear Carcinoma,Thymus Clear Cell Carcinoma,Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor,Essential Tremor,Central Nervous System Mesenchymal Non-Meningothelial Tumor,Congenital Fibrosarcoma,Autonomic Nervous System Neoplasm,Myoepithelioma,Endometrial Stromal Tumor,Sweat Gland Benign Neoplasm,Synovium Cancer,Small Intestinal Sarcoma,Bladder Leiomyoma,Extraskeletal Ewing Sarcoma,Lung Sarcoma,Endobronchial Lipoma,Cranial Nerve Malignant Neoplasm,Ring Chromosome,Biphasic Synovial Sarcoma,Epithelioid Cell Synovial Sarcoma,Well-Differentiated Liposarcoma,Cellular Myxoid Liposarcoma,Pleomorphic Liposarcoma,Peripheral Nervous System Disease,Small Cell Sarcoma,Sweat Gland Disease,Myxoid Chondrosarcoma,Skin Benign Neoplasm,Kidney Fibrosarcoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Myxoid Liposarcoma,Myasthenic Syndrome, Congenital, 5,Sarcoma,Mesenchymal Cell Neoplasm,Fibrosarcoma,Localized Osteosarcoma,Ewing Sarcoma Of Bone,Bone Osteosarcoma,Small Cell Osteogenic Sarcoma,Conventional Central Osteosarcoma,Cranial Nerve Neoplasm,Liposarcoma,Pediatric Fibrosarcoma,Congenital Myasthenic Syndrome,Olfactory Nerve Neoplasm,Rhabdoid Cancer,Kidney Rhabdoid Cancer,Olfactory Neuroblastoma,Extracranial Neuroblastoma,Extraskeletal Chondroma,Skeletal Muscle Cancer,Muscle Cancer,Sarcoma, Synovial,Askin'S Tumor,Ewing Sarcoma,Chondrosarcoma, Extraskeletal Myxoid,Cervical Neuroblastoma,Wilms Tumor 1,Connective Tissue Benign Neoplasm,Lipomatosis, Multiple

Cerebellar Ataxia Type 47,Spinocerebellar Ataxia 47

Spinal Muscular Atrophy

Diphtheria,Arthrogryposis, Renal Dysfunction, And Cholestasis 1

Systemic Scleroderma,Facial Hemiatrophy,Dyskinesia Of Esophagus,Connective Tissue Disease,Splenic Tuberculosis,Telangiectasis,Collagen Disease,Lupus Erythematosus,Childhood Type Dermatomyositis,Mixed Connective Tissue Disease,Limited Scleroderma,Diffuse Scleroderma,Raynaud Disease,Heart Block, Congenital,Hypotrichosis 13,Pericardium Disease,Autoimmune Disease Of Exocrine System,Crest Syndrome,Systemic Lupus Erythematosus,Syndromic X-Linked Intellectual Disability Cabezas Type

Gastrointestinal Lymphoma,Lymphomatoid Granulomatosis,Lymphomatoid Papulosis,Lethal Midline Granuloma,Viral Esophagitis,Myopathy,B-Cell Lymphoma,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Motor Neuron Disease,Orbit Lymphoma,Rhinosporidiosis,Angioimmunoblastic T-Cell Lymphoma,Leber Plus Disease,Amyotrophic Lateral Sclerosis 26 With Or Without Frontotemporal Dementia,Multisystem Proteinopathy,Dementia,Breast Lipoma,Reticulosarcoma,Sezary'S Disease,Aggressive Nk-Cell Leukemia,T-Cell Adult Acute Lymphocytic Leukemia,Giardiasis,Composite Lymphoma,Pediatric Lymphoma,Nasal Cavity Lymphoma,Primary Cutaneous Anaplastic Large Cell Lymphoma,Hepatosplenic T-Cell Lymphoma,Disease Of Mental Health,Panniculitis,Skin Disease,Welander Distal Myopathy,Erythema Multiforme,Lymphoma, Hodgkin, Classic,Lymphocytic Gastritis,Parasitic Ichthyosporea Infectious Disease,Mature T-Cell And Nk-Cell Lymphoma,Anaplastic Large Cell Lymphoma,Peripheral T-Cell Lymphoma,Lymphoma,Cutaneous T Cell Lymphoma,Lichen Sclerosus Et Atrophicus,Mycosis Fungoides,Lymphoproliferative Syndrome,Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood,Frontotemporal Dementia,Celiac Disease 1

Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy

Endometrial Stromal Sarcoma,Ocular Hypertension,Spinal Muscular Atrophy,Paralytic Poliomyelitis

Theileriasis,Spermatogenic Failure, X-Linked, 1

Follicular Adenoma,Retinitis Pigmentosa,Myopathy,Myotonic Dystrophy 1,Cervical Non-Keratinizing Squamous Cell Carcinoma,Periampullary Adenocarcinoma,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Juvenile Polyposis Syndrome,Disease Of Mental Health,Retinitis Pigmentosa 49,Scalp-Ear-Nipple Syndrome,Renal Cell Carcinoma, Nonpapillary

Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Myoblastoma,Autism Spectrum Disorder

Endometrial Stromal Sarcoma,Alzheimer Disease 5,Mouth Disease

Optic Nerve Disease,Ocular Hypertension,Hordeolum,Retinal Ischemia,Optic Nerve Hypoplasia, Bilateral

Brittle Bone Disorder

Charge Syndrome,Thymus Lymphoma,Microcephaly,Coloboma Of Macula,Verheij Syndrome,Xeroderma Pigmentosum, Complementation Group B,Neurodevelopmental Disorder With Hypotonia And Variable Intellectual And Behavioral Abnormalities

Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Patau Syndrome,Amyotrophic Lateral Sclerosis 1,Extracutaneous Mastocytoma,Indolent Systemic Mastocytosis,Spinal Muscular Atrophy,Sm-Ahnmd,Aggressive Systemic Mastocytosis,Leukemia, Acute Myeloid,Systemic Mastocytosis With Associated Hematologic Neoplasm,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Dilated Cardiomyopathy,Endometrial Stromal Tumor,Acute Megakaryoblastic Leukemia In Down Syndrome,Chronic Leukemia,Systemic Mastocytosis,Mastocytosis,Lactic Acidosis,Immune Deficiency Disease,Myelodysplastic Syndrome,Down Syndrome,Holt-Oram Syndrome,Myelofibrosis,Atypical Chronic Myeloid Leukemia,Melanoma, Uveal

Follicular Adenoma,Ulcerative Blepharitis,Chromosome 4q21 Deletion Syndrome

Endometrial Stromal Sarcoma,Myopathy,Bulbar Polio,Atrial Septal Defect 1,Human T-Cell Leukemia Virus Type 2,Patellar Tendinitis,Congenital Myasthenic Syndrome,Mouth Disease,Paralytic Poliomyelitis,Atrial Septal Defect 2,Frontotemporal Dementia

Atrial Septal Defect 1,Optic Nerve Neoplasm,Autism

Perlman Syndrome,Retinitis Pigmentosa,Extraocular Retinoblastoma,Renal Wilms' Tumor,Sleeping Sickness,Poikiloderma With Neutropenia,Trichothiodystrophy 2, Photosensitive

Endometrial Stromal Sarcoma,Spinal Muscular Atrophy,Muscular Atrophy,Endometrial Stromal Tumor,Frontotemporal Dementia

Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Myopathy,Homocystinuria,Rothmund-Thomson Syndrome, Type 2,Endometrial Stromal Tumor,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Retinitis Pigmentosa 4,Congenital Myasthenic Syndrome,Alzheimer Disease 3

Dysostosis,Synostosis,Burn-Mckeown Syndrome,Phocomelia,Radioulnar Synostosis,Charcot-Marie-Tooth Disease X-Linked Recessive 4,Hereditary Hearing Loss And Deafness,Usher Syndrome, Type Iia,Cerebrocostomandibular Syndrome,Cleft Palate, Isolated,Mandibulofacial Dysostosis, Guion-Almeida Type,Ehlers-Danlos Syndrome, Classic Type, 1,Humeroradial Synostosis,Acrofacial Dysostosis Syndrome Of Rodriguez,Acrofacial Dysostosis,Acrofacial Dysostosis 1, Nager Type,Treacher Collins Syndrome 1,Postaxial Acrofacial Dysostosis

Partial Deletion Of Y,Male Infertility,Y Chromosome Infertility,Testicular Germ Cell Cancer,Myotonic Dystrophy 2,Azoospermia,Spermatogenic Failure, Y-Linked, 2,Gonadoblastoma

Chondrosarcoma,Extraskeletal Mesenchymal Chondrosarcoma,Extraosseous Chondrosarcoma,Amyotrophic Lateral Sclerosis 1,Acute Leukemia,Intracranial Chondrosarcoma,Multisystem Proteinopathy,Lung Sarcoma,Myxoid Chondrosarcoma,Liposarcoma,Ewing Sarcoma,Chondrosarcoma, Extraskeletal Myxoid,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4,Bone Chondrosarcoma

Amyotrophic Lateral Sclerosis 6 With Or Without Frontotemporal Dementia,Lattice Corneal Dystrophy,Tremor, Hereditary Essential, 4,Amyotrophic Lateral Sclerosis 18,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Anal Carcinoma In Situ,Amyotrophic Lateral Sclerosis 11,Clear Cell Sarcoma,Tremor,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Neuromuscular Disease,Fibrous Histiocytoma,Connective Tissue Cancer,Progressive Bulbar Palsy,Pica Disease,Dysgraphia,Nominal Aphasia,Extraosseous Chondrosarcoma,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Ideomotor Apraxia,Giant Axonal Neuropathy 2,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Movement Disease,Muscular Atrophy,Locked-In Syndrome,Essential Tremor,Multisystem Proteinopathy,Synovium Cancer,Dementia,Cerebellar Disease,Juvenile Amyotrophic Lateral Sclerosis,Chondroid Lipoma,Dystonia,Myeloid Leukemia,Tremor, Hereditary Essential, 2,Well-Differentiated Liposarcoma,Cellular Myxoid Liposarcoma,Pediatric Liposarcoma,Pleomorphic Liposarcoma,Mixed Liposarcoma,Sclerosing Liposarcoma,Amyotrophic Lateral Sclerosis 4, Juvenile,Speech And Communication Disorders,Progressive Muscular Atrophy,Kidney Fibrosarcoma,Rhabdomyosarcoma,Pick Disease Of Brain,Myxoid Liposarcoma,Autosomal Dominant Cerebellar Ataxia,Sarcoma,Fibrosarcoma,Liposarcoma,Disease Of Mental Health,Dentatorubral-Pallidoluysian Atrophy,Dermatopathia Pigmentosa Reticularis,Dementia, Lewy Body,Hemochromatosis, Type 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Sarcoma, Synovial,Spinocerebellar Ataxia 2,Tremor, Hereditary Essential, 3,Amyotrophic Lateral Sclerosis 21,Amyotrophic Lateral Sclerosis 9,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia,Tremor, Hereditary Essential, 1,Ewing Sarcoma,Amyotrophic Lateral Sclerosis 16, Juvenile,Chondrosarcoma, Extraskeletal Myxoid,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Epilepsy, Familial Temporal Lobe, 8,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Autism Spectrum Disorder,Aphasia,Writing Disorder,Associative Agnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 12,Amyotrophic Lateral Sclerosis Type 14,Lipomatosis, Multiple,Amyotrophic Lateral Sclerosis Type 22,Epithelial-Stromal Tgfbi Dystrophy,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7

Episodic Ataxia, Type 6

Lung Cancer

Epilepsy,Atrial Heart Septal Defect,Myopia,Undetermined Early-Onset Epileptic Encephalopathy,Focal Epilepsy,Refractive Error,Developmental Coordination Disorder,Atrial Septal Defect 1,Conduct Disorder,Colorectal Cancer,Autosomal Dominant Cerebellar Ataxia,Benign Epilepsy With Centrotemporal Spikes,Disease Of Mental Health,Wheat Allergy,Dengue Shock Syndrome,Schizophrenia,Spinocerebellar Ataxia 2,Attention Deficit-Hyperactivity Disorder,Pervasive Developmental Disorder,Autism Spectrum Disorder,Atrial Septal Defect 2,Rett Syndrome,Autism,Epilepsy, Idiopathic Generalized

Pancreatic Adenocarcinoma,Ovarian Mucinous Neoplasm,Muscular Disease,Skin Melanoma,Heart Septal Defect,X-Linked Recessive Disease,Chromosomal Disease,Uterine Body Mixed Cancer,Uterine Carcinosarcoma,Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Lung Cancer Susceptibility 3,Urinary System Disease,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Patau Syndrome,Erythromelalgia,Mast-Cell Leukemia,Suppression Of Tumorigenicity 12,Connective Tissue Disease,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,Pleuropulmonary Blastoma,Non-Langerhans-Cell Histiocytosis,Splenic Sequestration,Muscle Tissue Disease,Autoimmune Disease Of The Nervous System,Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency,Nephroma,Kidney Cortex Disease,Spleen Cancer,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Leukocyte Disease,Hemosiderosis,Amyloidosis, Finnish Type,Mature B-Cell Neoplasm,Amyotrophic Lateral Sclerosis 1,Ovary Epithelial Cancer,Ocular Cancer,Blood Platelet Disease,Extracutaneous Mastocytoma,Indolent Systemic Mastocytosis,Essential Thrombocythemia,Myeloproliferative Neoplasm,Infratentorial Cancer,Monoclonal Gammopathy Of Uncertain Significance,Eye Degenerative Disease,Lymphatic System Disease,Female Reproductive System Disease,Endocervical Carcinoma,Motor Neuron Disease,Shigellosis,Sm-Ahnmd,Aggressive Systemic Mastocytosis,Male Reproductive System Disease,Leukemia,Pancytopenia,Mixed Phenotype Acute Leukemia,Myelophthisic Anemia,Blood Coagulation Disease,Macrocytic Anemia,Wernicke Encephalopathy,Acquired Von Willebrand Syndrome,Neutrophilia, Hereditary,Bronchiolo-Alveolar Adenocarcinoma,Adenocarcinoma In Situ,Leukemia, Acute Myeloid,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Splenic Disease,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Dendritic Cell Deficiency,Pancreas Disease,Thoracic Cancer,Autonomic Nervous System Neoplasm,Endometrial Stromal Tumor,Transitional Cell Carcinoma,Hepatic Vascular Disease,Dyskeratosis Congenita,Cerebellar Disease,Endocrine System Disease,Colonic Disease,Hairy Cell Leukemia,Cervix Carcinoma,Immune System Disease,Buschke-Ollendorff Syndrome,Chronic Leukemia,Nervous System Disease,Diamond-Blackfan Anemia,Aplastic Anemia,Myeloid Sarcoma,Myeloid Leukemia,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Acute Megakaryocytic Leukemia,Anemia, Congenital Dyserythropoietic, Type Ii,Transcobalamin Ii Deficiency,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Pelger-Huet Anomaly,Testis Seminoma,Demyelinating Disease,Refractory Cytopenia With Multilineage Dysplasia,Germinoma,Central Nervous System Disease,Deficiency Anemia,Meckel Syndrome, Type 2,Qualitative Platelet Defect,Fanconi Anemia, Complementation Group A,Histiocytosis,Breast Adenocarcinoma,Uveal Disease,Reproductive System Disease,Disease Of Mental Health,Cervical Cancer,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Respiratory System Disease,Bladder Disease,Thrombocytopenia,Mast Cell Neoplasm,Integumentary System Disease,Skin Disease,Retinitis Pigmentosa 23,Type 1 Diabetes Mellitus 2,Langerhans Cell Histiocytosis,Sensory System Disease,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Odontochondrodysplasia,Severe Congenital Neutropenia,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Respiratory System Cancer,Immune Deficiency Disease,Myelodysplastic Syndrome,X-Linked Monogenic Disease,Autosomal Recessive Disease,Autosomal Genetic Disease,Marginal Zone B-Cell Lymphoma,Anemia, Sideroblastic, And Spinocerebellar Ataxia,Uterine Anomalies,Uterine Corpus Endometrial Carcinoma,Endocervical Adenocarcinoma,Wilms Tumor 1,Autosomal Recessive Cerebellar Ataxia,Autoimmune Disease Of Central Nervous System,Specific Developmental Disorder,Pontocerebellar Hypoplasia, Type 1b,Lymphatic System Cancer,Leukemia, Acute Monocytic,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Psoriasis 9,Atrial Septal Defect 2,Chromosomal Duplication Syndrome,Myelofibrosis,Myeloma, Multiple,Spinal Disease,Atypical Chronic Myeloid Leukemia,Melanoma, Uveal,Isolated Growth Hormone Deficiency,Microcephalic Osteodysplastic Primordial Dwarfism, Type I,Autosomal Dominant Non-Syndromic Intellectual Disability 3,Lung Cancer,Shwachman-Diamond Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia,Polycythemia Vera

Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Blood Platelet Disease,Endometrial Mixed Adenocarcinoma,Blood Coagulation Disease,Orofaciodigital Syndrome X,Thrombocytopenia-Absent Radius Syndrome,Thoracic Outlet Syndrome,Usher Syndrome, Type I,Microcephaly,Pick Disease Of Brain,Disease Of Mental Health,Thrombocytopenia,Amegakaryocytic Thrombocytopenia, Congenital,Dystonia 16,Holt-Oram Syndrome,Cardiomyopathy, Dilated, 1m

Supranuclear Palsy, Progressive, 1,Mutism,Myopathy,Amyotrophic Lateral Sclerosis 11,Akinetic Mutism,Myofibrillar Myopathy,Neuromuscular Disease,Alzheimer Disease,Pica Disease,Dysgraphia,Nominal Aphasia,Amyotrophic Lateral Sclerosis 1,Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Ideomotor Apraxia,Giant Axonal Neuropathy 2,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Movement Disease,Muscular Atrophy,Dyscalculia,Distal Hereditary Motor Neuronopathy Type 7,Pseudobulbar Palsy,Locked-In Syndrome,Prosopagnosia,Machado-Joseph Disease,Arteriolosclerosis,Multisystem Proteinopathy,Semantic Dementia,Dementia,Tardbp-Related Amyotrophic Lateral Sclerosis,Alexia,Amyotrophic Lateral Sclerosis 4, Juvenile,Perry Syndrome,Speech And Communication Disorders,Progressive Muscular Atrophy,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Autosomal Dominant Cerebellar Ataxia,Amyotrophic Lateral Sclerosis 19,Niemann-Pick Disease,Liposarcoma,Disease Of Mental Health,Masp2 Deficiency,Dermatopathia Pigmentosa Reticularis,Dementia, Lewy Body,Fragile X Syndrome,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Ophthalmomyiasis,Spinocerebellar Ataxia 2,Nonaka Myopathy,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4,Huntington Disease,Epilepsy, Idiopathic Generalized 2,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Aphasia,Writing Disorder,Inclusion Body Myositis,Associative Agnosia,Simultanagnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 12,Agraphia,Neuronopathy, Distal Hereditary Motor, Type Viib,Amyotrophic Lateral Sclerosis, Juvenile, With Dementia,Amyotrophic Lateral Sclerosis Type 22,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7

Enchondroma,Pilomyxoid Astrocytoma,Pilocytic Astrocytoma,Adenocarcinoma In Situ,Pancreatic Cancer

Chronic Interstitial Cystitis,Chromosomal Disease,Mononeuritis Multiplex,Dyskinesia Of Esophagus,Connective Tissue Disease,Potocki-Shaffer Syndrome,Diffuse Infiltrative Lymphocytosis Syndrome,Mononeuropathy,Hemorrhagic Disease,Sjogren Syndrome,Polyclonal Hypergammaglobulinemia,Keratoconjunctivitis Sicca,Submandibular Gland Disease,Xerophthalmia,Heart Conduction Disease,Parotitis,Parotid Disease,Sialadenitis,Uveoparotid Fever,Orbital Granuloma,Undifferentiated Connective Tissue Disease,Lupus Erythematosus,Mononeuritis Of Upper Limb And Mononeuritis Multiplex,Lacrimal Apparatus Disease,Salivary Gland Disease,Endocardial Fibroelastosis,Hepatitis C Virus,Limited Scleroderma,Raynaud Disease,Heart Block, Congenital,Atrioventricular Block,Second-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Lymphoid Interstitial Pneumonia,Autoimmune Disease Of Exocrine System,Autoimmune Disease Of Musculoskeletal System,Munchausen By Proxy,Systemic Lupus Erythematosus,Chromosomal Deletion Syndrome

Dyslexia,Childhood Kidney Cell Carcinoma,Parkinson Disease, Late-Onset,Pick Disease Of Brain,Perivascular Tumor,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Xp11-Associated,Frontotemporal Dementia

Spinocerebellar Ataxia 1,Autosomal Dominant Cerebellar Ataxia,Dentatorubral-Pallidoluysian Atrophy

Metaphyseal Chondrodysplasia, Schmid Type,Retinitis Pigmentosa

Lattice Corneal Dystrophy,Endometrial Stromal Sarcoma,Myopathy,Amyotrophic Lateral Sclerosis 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Autosomal Dominant Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Muscular Atrophy,Relapsing-Remitting Multiple Sclerosis,Atrial Septal Defect 1,Human T-Cell Leukemia Virus Type 2,Endometrial Stromal Tumor,Oculopharyngeal Muscular Dystrophy,Multisystem Proteinopathy,Dementia,Paget'S Disease Of Bone,Burkitt Lymphoma,Colorectal Cancer,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3,Amyotrophic Lateral Sclerosis 20,Disease Of Mental Health,Dermatopathia Pigmentosa Reticularis,Multiple Sclerosis,Spinocerebellar Ataxia 2,Immune Deficiency Disease,Secondary Progressive Multiple Sclerosis,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Inflammatory Myofibroblastic Tumor,Epithelial-Stromal Tgfbi Dystrophy,Frontotemporal Dementia

Achalasia-Addisonianism-Alacrima Syndrome,Seminal Vesicle Tumor,Male Reproductive Organ Benign Neoplasm,Lethal Congenital Contracture Syndrome 1

Chromosome 22q11.2 Deletion Syndrome, Distal

Mirror Movements 1,Atrial Septal Defect 5,Fundus Dystrophy,Ileocolitis,Deafness, Autosomal Recessive 37

Diamond-Blackfan Anemia 2,Corneal Dystrophy, Avellino Type

Muscular Disease,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Autosomal Dominant Distal Myopathy,Muscular Dystrophy,Noonan Syndrome 1,Oculopharyngeal Muscular Dystrophy,Influenza,Dysphagia,Hand-Foot-Genital Syndrome,Partington X-Linked Mental Retardation Syndrome,Ptosis,Central Hypoventilation Syndrome, Congenital,Frontotemporal Dementia