1833
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Chromodomain helicase DNA binding protein 6 |
CHD-6, CHD5, RIGB |
Curated: Transitional cell carcinoma, Diabetes mellitus, Hallermanns syndrome, Hallervorden spatz syndrome, Major depressive disorder, Neuroblastoma, Prostatic neoplasms, Urinary bladder neoplasms
Unreviewed: Adenoma, Astigmatism, Autism Spectrum Disorder, Azoospermia, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Heart Disease, Craniosynostosis, Cystic fibrosis, Developmental disability, Down Syndrome, Endometriosis, Epilepsy, Gallbladder cancer, Glioblastoma, Glioma, Hepatocellular carcinoma, Hereditary cutaneous melanoma, Hypersensitivity, Infantile spasms, Intellectual developmental disorder, Language development disorders, Laryngeal Carcinoma, Learning disorders, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lymphatic metastasis, Lymphoma, Malignant Neoplasm, Melanoma, Mental retardation, Neoplasms, Neurodegenerative Disorders, Ovarian cancer, Ovarian diseases, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatitis, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Rectal Carcinoma, Renal Carcinoma, Renal cell carcinoma, Seizures, Stomach Carcinoma, Stomach Neoplasms, Tarsal-Carpal Coalition Syndrome, Urinary bladder cancer
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1834
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Chromodomain helicase DNA binding protein 7 |
CRG, HH5, IS3, KAL5 |
Curated: Angioedema, Atrial septal defect, Atrioventricular septal defect, Attention deficit hyperactivity disorder, Dilated cardiomyopathy, Charge syndrome, Choanal atresia syndrome, Coloboma, Congenital pulmonary artery atresia, Craniofacial ulnar renal syndrome, Developmental disability, Hearing loss, Hyperopia, Hypogonadotropic hypogonadism, Hypopituitarism, Hypothyroidism, Growth hormone deficiency, Insomnia, Kallmann syndrome, Major depressive disorder, Male infertility spermatogenesis disorder, Myopia, Neurodevelopmental disorder, Omenn syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Prostate cancer, Prostatic neoplasms, Scoliosis, Sheehan syndrome, Substance abuse, Swyer syndrome, Systemic sclerosis, Tetralogy of fallot, Wiedemann-steiner syndrome
Unreviewed: 46, xy disorder of sex development, Absence Of Septum Pellucidum, Adrenocorticotropic Hormone Deficiency, Alopecia, Androgen insensitivity syndrome, Anemia, Aneurysm Of Aortic Arch, Angina pectoris, Anodontia, Anxiety Disorder, Aortic Coarctation, Aplasia of the thymus, Aqueductal Stenosis, Asymmetric crying face association, Atrial Septal Defect, Attention Deficit Hyperactivity Disorder, Autism, Autism Spectrum Disorder, Autoimmune lymphoproliferative disorder, Azoospermia, Brachial plexus neuritis, Brachycephaly, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast hypoplasia, Breast neoplasm, Camptodactyly of fingers, Cardiomyopathy, Cardiovascular Diseases, Carotid artery disease, Cartilage-Hair Hypoplasia, Cerebellar Hypoplasia, Cerebellar vermis agenesis, Cerebrovascular disorder, CHARGE Syndrome, Choanal Atresia, Ciliary dyskinesia, Cleft lip, Cleft Palate And Bilateral Cleft Lip, Cleft palate with coloboma of eye and deafness, Cognition disorder, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Combined pituitary hormone deficiency, Congenital abnormalities, Congenital anosmia, Congenital Atresia Of Pulmonary Artery, Congenital Camptodactyly, Congenital central hypoventilation syndrome, Congenital Chromosomal Disease, Congenital Coloboma Of Iris, Congenital Epicanthus, Congenital Exomphalos, Congenital heart defect, Congenital heart defects, Congenital Hypogonadotropic Hypogonadism, Congenital Hypothyroidism, Congenital Malformation Syndrome, Congenital Musculoskeletal Anomalies, Congenital myopathy, Congenital ocular coloboma, Congenital omphalocele, Congenital Sensorineural Hearing Loss, Conotruncal defect, Contiguous gene syndrome, Craniofacial abnormalities, Craniosynostosis, Cryptorchidism, Dandy-Walker Syndrome, Deafness, Development Disorder, Developmental Delay, DiGeorge Syndrome, Disorders of sex development, Dolichocephaly, Double Outlet Right Ventricle, Duane Retraction Syndrome, Duodenal Atresia, Dwarfism, Dysarthria, Dysmorphic Features, Dysphagia, Ear disease, Endometrial neoplasm, Endometrioid carcinoma, Eosinophilia, Epilepsy, Erectile Dysfunction, Esophageal Atresia, Exfoliative Dermatitis, Facial paralysis, Facioscapulohumeral muscular dystrophy, Female Hypogonadism Syndrome, Fragile X Syndrome, Frontonasal Dysplasia, Fundus Coloboma, Gastroesophageal Reflux Disease, Glioblastoma, Glioma, Goldenhar Syndrome, Gonadotropin Deficiency, Growth disorder, Gynecomastia, Hearing Loss, Heart Diseases, Heart Septal Defects, Hepatocellular carcinoma, Holoprosencephaly, Horizontal gaze palsy with progressive scoliosis, Horseshoe Kidney, Hydrocephalus, Hydronephrosis, Hypertension, Hypoaldosteronism, Hypogonadism, Hypogonadotropic Hypogonadism, Hypogonadotropic Hypogonadism With Or Without Anosmia, Hypoparathyroidism, Hypoplasia Of Corpus Callosum, Hypoplasia of the ovary, Hypoplasia Of Thumb, Hypospadias, Ichthyosis, Immunologic Deficiency Syndromes, Impaired Cognition, Imperforate anus, Infertility, Intellectual developmental disorder, Interrupted aortic arch, Isolated Somatotropin Deficiency, Kabuki Syndrome, Kallmann Syndrome, Kaposi Sarcoma, Kartagener Syndrome, Laryngeal hypoplasia, Laryngomalacia, Learning disorders, Liver neoplasm, Lobar Holoprosencephaly, Lung neoplasms, Lymphoma, Lymphopenia, Male infertility, Malignant Neoplasm, Mandibulofacial Dysostosis, Medulloblastoma, Mental Depression, Mental retardation, Metabolic Myopathy, Microcephaly, Micrognathism, Micropenis, Microphthalmia, Microphthalmos, Microstomia, Microtia, Migraine, Mirror Movements, Movement Disorders, Multiple Congenital Anomalies, Multiple myeloma, Myasthenic Syndrome, Myeloid leukemia, Myofibrillar myopathy, Myopathy, Neck Webbing, Neoplasms, Nephrotic Syndrome, Neurodevelopmental Disorders, Non-obstructive azoospermia, Noonan syndrome, Normosmic Congenital Hypogonadotropic Hypogonadism, Nystagmus, Obesity, Obsessive-Compulsive Disorder, Omenn Syndrome, Optic Atrophy, Orofaciodigital syndrome, Osteochondrodysplasia, Osteopenia, Osteoporosis, Otitis media, Pancreatic cancer, Pancreatic carcinoma, Papillary thyroid cancer, Paraplegia, Parathyroid hypoplasia, Patent ductus arteriosus, Penile Hypospadias, Penis Agenesis, Periodontitis, Physiologic Amenorrhea, Posteriorly Rotated Ear, Prostatic Neoplasms, Prune belly syndrome, Ptosis, Pulmonary hypertension, Pulmonary Stenosis, Radial Aplasia, Renal agenesis, Renal hypoplasia, Retinal coloboma, Rheumatoid arthritis, Secondary Physiologic Amenorrhea, Septo-Optic Dysplasia, Severe combined immunodeficiency, Severe combined immunodeficiency disease, Shprintzen-Goldberg Syndrome, Skeletal Dysplasia, Somatotropin Deficiency, Squamous cell carcinoma, Stomach neoplasms, Strabismus, Stroke, Syndactyly, Syndromic microphthalmia, Talipes, Teratoma, Testicular Hypogonadism, Tetralogy of Fallot, Thyroid Agenesis, Thyroid cancer, Thyroiditis, Tracheal Stenosis, Transposition Of Great Vessels, Trichohepatoenteric Syndrome, Triple negative breast cancer, Tubular Aggregate Myopathy, Uranostaphyloschisis, Urinary bladder neoplasms, Urogenital abnormalities, Uveal melanoma, Vacterl association, Vascular disease, Ventricular outflow obstruction, Ventricular septal defect, Vesicoureteral Reflux, Visual disorder, Vitamin A Deficiency, Waardenburg Syndrome
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1835
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Chromodomain helicase DNA binding protein 8 |
AUTS18, HELSNF1, IDDAM |
Curated: 14q11.2 microduplication syndrome, Anxiety disorder, Autism, Chromodomain helicase dna binding protein 8 overgrowth syndrome, Color vision deficiency, Neurodevelopmental disorder, Congenital myasthenic syndrome, Congenital ptosis, Developmental delay, Developmental disability, Digestive system disease, Gastrointestinal disease, Intellectual developmental disorder autism dysmorphic, Intellectual developmental disorder, Myasthenic syndrome, Non-specific syndromic intellectual disability, complex neurodevelopmental disorder
Unreviewed: Autism spectrum disorder, Bipolar disorder, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Burkitt lymphoma, Cardiovascular Diseases, CHARGE Syndrome, Cholangiocarcinoma, Colorectal Cancer, Developmental Delay, Diabetes Mellitus, Dysmorphic Features, Dyssomnia, Dystonia, Eczema, Functional Gastrointestinal Disorders, Gastrointestinal Diseases, Growth disorder, Hematopoietic Neoplasms, Hepatocellular carcinoma, Leukemia, Lymphoblastic Leukemia, Lymphoma, Macrocephaly, Malignant Neoplasm, Mental retardation, Metastatic Prostate Carcinoma, Microcephaly, Multiple Congenital Anomalies, Neoplasms, Neurodevelopmental Disorders, Obesity, Ocular albinism, Prostate cancer, Prostatic neoplasm, Schizophrenia, Seizures, Sleep Disorders, Stomach Carcinoma, Stomach Neoplasms, Stroke, Triple negative breast cancer, Ulerythema ophryogenesis
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1836
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Chromodomain helicase DNA binding protein 9 |
AD013, CHD-9, CReMM, KISH2, PRIC320 |
Curated: Coronary artery disease, Ocular hypertension, Pelvic organ prolapse, Systemic lupus erythematosus, Venous thromboembolism
Unreviewed: Colorectal Cancer, Colorectal neoplasm, Developmental disability, Hypertension, Malignant Neoplasm, Myocardial Ischemia, Neoplasms, Neuroblastoma, Obesity, Werner Syndrome
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1838
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Choline dehydrogenase |
- |
Curated: Cardiovascular disease, Congestive heart failure, Heart failure, Hypertension
Unreviewed: Androgen insensitivity syndrome, Anodontia, Anxiety Disorder, Aortic Aneurysm, Aortic Valve Sclerosis, Arteriosclerosis, Arthritis, Atherosclerosis, Atrial Septal Defect, Atrioventricular septal defect, Autism Spectrum Disorder, Bipolar Disorder, Bone Marrow Diseases, Borderline personality disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, Cardiomyopathy, Cardiovascular Diseases, Cerebrovascular Disorders, CHARGE Syndrome, Cholecystitis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Complete Atrioventricular Block, Complete Atrioventricular Canal Defect, Congenital Atresia Of Pulmonary Artery, Congenital Atresia Of Pulmonary Valve, Congenital Chromosomal Disease, Congenital diaphragmatic hernia, Congenital heart defects, Congenital Heart Disease, Congestive Heart Failure, Conotruncal defect, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Cystic Fibrosis, Developmental dysplasia of the hip, Diabetes, Diabetes Mellitus, Double Outlet Right Ventricle, Down Syndrome, Dyslipidemias, Ebstein anomaly of the tricuspid valve, Embryonal carcinoma, Epilepsy, Esophageal Carcinoma, Esophageal neoplasm, Esophagus Neoplasm, Fabry disease, Fuchs Endothelial Dystrophy, Gastrointestinal stromal tumor, Glaucoma, Hashimoto Disease, Heart Diseases, Heart Failure, Hypercholesterolemia, Hyperhomocysteinemia, Hyperlipidemia, Hyperlipoproteinemia, Hypodontia, Hypoplastic Left Heart Syndrome, Impaired Cognition, Intervertebral disc disease, Ischemic Stroke, Kidney Disease, Kidney Failure, Lipid Metabolism Disorders, Liver carcinoma, Liver Fibrosis, Malignant Neoplasm, Mammary Neoplasms, Mental Depression, Mental retardation, Metabolic Syndrome, Microvascular Angina, Myocardial Infarction, Myocardial Ischemia, Necrotizing Enterocolitis, Neoplasms, Non-Alcoholic Fatty Liver Disease, Obesity, Pancreatic neoplasm, Parkinson disease, Patent foramen ovale, Peripheral arterial stenosis, Precocious puberty, Premature Menopause, Pulmonary arterial hypertension, Pulmonary Hypertension, Pulmonary venoocclusive disease, Respiration Disorders, Respiratory Tract Diseases, Rickets, Schizophrenia, Secundum atrial septal defect, Spinal Cord Diseases, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Stroke, Tetralogy of Fallot, Thyroid Diseases, Trichohepatoenteric Syndrome, Vascular Diseases, Ventricular septal defect, Vitamin D Deficiency
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