768
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AT-hook DNA binding motif containing 1 |
MRD25, XIGIS |
Curated: Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Coronary artery disease, Global developmental delay, Intellectual developmental disorder, Myocardial infarction, Neurodevelopmental disorder, Psoriasis, Sleep apnea, Xia-gibbs syndrome, AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome
Unreviewed: Central Visual Impairment, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Congenital Heart Disease, Craniosynostosis, Development Disorder, Developmental Delay, Developmental disability, Epilepsy, Esotropia, Hypersensitivity, Hypoplasia Of Corpus Callosum, Hypotonia, Intellectual Disability-Obstructive Sleep Apnea-Mild Dysmorphism Syndrome, Language development disorders, Laryngomalacia, Mental retardation, Metabolic syndrome, Micrognathism, Neurodevelopmental Disorders, Pancreatic ductal carcinoma, Pituitary dwarfism, Scoliosis, Seizures, Sleep Apnea, Submucosal cleft palate, Uterine neoplasm, Visual disorder, Xia-Gibbs syndrome
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769
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Abelson helper integration site 1 |
AHI-1, JBTS3, ORF1, dJ71N10.1 |
Curated: Asthma, Eczema, Autism, Cerebellar diseases, Clonal hematopoiesis, Aplasia of the vermis, Global developmental delay, Hodgkin lymphoma, Selective immunoglobulin a deficiency, Intellectual developmental disorder, Joubert syndrome, Juvenile idiopathic arthritis, Leber congenital amaurosis, Multiple sclerosis, Nephronophthisis, Nephrotic syndrome, Optic atrophy, Peripheral arterial disease, Respiratory system disease, Retinal degeneration, Retinitis pigmentosa, Rod-cone dystrophy, Schizophrenia, Selective iga deficiency disease, Systemic lupus erythematosus, joubert syndrome 3
Unreviewed: Agenesis Of Corpus Callosum, Aicardi goutieres syndrome, Angioimmunoblastic T-cell lymphoma, Anxiety Disorder, Apraxia, Attention deficit hyperactivity disorder, Autism Spectrum Disorder, B-Cell Lymphoma, Basal cell carcinoma, Bipolar Disorder, Bladder carcinoma, Brain malformation, Breast neoplasm, Cataract, Cerebellar Diseases, Cerebellar vermis agenesis, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Ciliopathies, Ciliopathy, Classical Hodgkin lymphoma, Cognitive disorder, Colorectal Cancer, Cone-rod dystrophy, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Epicanthus, Congenital Hypoplasia Of Penis, Cystic Kidney Disease, Development Disorder, Developmental Delay, Developmental disability, Dextrocardia, Diabetes Mellitus, Diabetes mellitus, type 2, Disorder Of Eye, Epileptic encephalopathy, Fibrosarcoma, Fulminant Hepatitis, Fundus Coloboma, Gastroenteritis, Glaucoma, Glioblastoma, Glioma, Hearing Loss, Hematological Disease, Hepatitis c, Hirschsprung Disease, Hodgkin Disease, Huntington Disease, Hydatidiform mole, Hydrocephalus, Hyperinsulinism, Hypogonadism, Immunoglobulin A deficiency, Impaired Cognition, Intraductal noninfiltrating carcinoma, Jacobsen Syndrome, Johanson-Blizzard Syndrome, Joubert Syndrome, Joubert Syndrome With Ocular Defect, Keratoconus, Kidney Disease, Leukemia, Liver carcinoma, Lupus Erythematosus, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphoma, Malignant Neoplasm, Meckel-gruber syndrome, Melanoma, Mental Depression, Mental Disorders, Mental retardation, Metabolic Syndrome, Multiple Sclerosis, Myeloid Leukemia, Neoplasm, Neoplasms, Nephrotic Syndrome, Neuroblastoma, Neurodevelopmental Disorders, Nonorganic Psychosis, Nystagmus, Obesity, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Oral cleft, Ovarian neoplasm, Pancreatic ductal carcinoma, Polydactyly, Polydactyly Of Toes, Polymicrogyria, Psychosis, Ptosis, Respiratory Tract Diseases, Retinal coloboma, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Rheumatoid arthritis, Rhyns syndrome, Scoliosis, Selective Immunoglobulin A Deficiency, Sezary Syndrome, Situs Inversus, Skin neoplasm, Sleep Apnea, Squamous cell carcinoma, Strabismus, T-cell leukemia, T-Cell Lymphoma/Leukemia, Thymoma, Trichohepatoenteric Syndrome, Urinary bladder neoplasms, Ventricular septal defect
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770
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AHI1 divergent transcript |
C6orf217, LINC00271, NCRNA00271 |
Curated: N/A
Unreviewed: Adrenocortical carcinoma, Alzheimer disease, Autoimmune Diseases, Bipolar Disorder, Diabetes Mellitus, Hypothyroidism, Malignant Neoplasm, Neoplasms, Papillary thyroid carcinoma, Schizophrenia
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