Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
941 to 950 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

941
Chromodomain helicase DNA binding protein 2
DEE94, EEOC
Alzheimer disease, Autism, Neurodevelopmental disorder, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Epilepsy with myoclonic atonic seizures, Rolandic epilepsy, Glomerulonephritis, Intellectual developmental disorder, Lennox-gastaut syndrome, Lung cancer, Non-specific syndromic intellectual disability, Osteoarthritis, Schizophrenia

942
Chromodomain helicase DNA binding protein 3
Mi-2a, Mi2-ALPHA, SNIBCPS, ZFH
Breast cancer, Cancer, Basal cell carcinoma, Colorectal cancer, Estrogen-receptor negative breast cancer, Global developmental delay, Gout, Intellectual developmental disorder, Lung cancer, Neurodevelopmental disorder, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Prostatic neoplasms, Sezary syndrome
View all (2 more)

943
Chromodomain helicase DNA binding protein 4
CHD-4, Mi-2b, Mi2-BETA, SIHIWES
Atrial fibrillation, Autism, Developmental disability, Endometrial neoplasms, Genetic predisposition to disease, Global developmental delay, Lung neoplasms, Metabolic syndrome, Schizophrenia, Stomach neoplasms, Tetralogy of fallot, Diabetes mellitus type 2

944
Chromodomain helicase DNA binding protein 5
CHD-5, PMNDS
Central nervous system cancer, Colorectal neoplasms, Crohn disease, Glioblastoma, Glioma, Global developmental delay, Inflammatory bowel disease, Intellectual developmental disorder, Neuroblastoma, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Ocular anomalies with axonal neuropathy and developmental delay, Parenti-mignot neurodevelopmental syndrome, Schizophrenia

945
Chromodomain helicase DNA binding protein 6
CHD-6, CHD5, RIGB
Transitional cell carcinoma, Diabetes mellitus, Hallermanns syndrome, Hallervorden spatz syndrome, Major depressive disorder, Neuroblastoma, Prostatic neoplasms, Urinary bladder neoplasms

946
Chromodomain helicase DNA binding protein 7
CRG, HH5, IS3, KAL5
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 impairment, Hyperopia, Hypogonadotropic hypogonadism, Hypopituitarism
View all (22 more)

947
Chromodomain helicase DNA binding protein 8
AUTS18, HELSNF1, IDDAM
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
View all (1 more)

948
Chromodomain helicase DNA binding protein 9
AD013, CHD-9, CReMM, KISH2, PRIC320
Coronary artery disease, Ocular hypertension, Pelvic organ prolapse, Systemic lupus erythematosus, Venous thromboembolism

949
CHD9 neighbor
PR-lncRNA-1
Liver cirrhosis

950
Choline dehydrogenase
-
Cardiovascular disease, Congestive heart failure, Heart failure, Hypertension