|
371
|
|
|
CAMP responsive element binding protein 1 |
CREB, CREB-1 |
|
|
372
|
|
|
CREB binding lysine acetyltransferase |
CBP, KAT3A, MKHK1, RSTS, RSTS1 |
Adenocarcinoma, Agenesis of corpus callosum, Agoraphobia, Amyotrophic lateral sclerosis, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Avascular necrosis of the capital femoral epiphysis, Urinary bladder cancer, Bladder neoplasm, Camptodactyly of fingers, Carcinoma, Carcinoma of the head and neck, Cataract, Uterine cervix neoplasm, Chorioretinal dystrophy, Colorectal neoplasms, Dislocated radial head, Congenital epicanthus, Congenital ocular coloboma, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Dental enamel hypoplasia, Developmental delay, Diffuse lymphoma, Duane retraction syndrome, Dwarfism, Dysmorphic features, Esophagus neoplasm, Frontal bossing, Gastric cancer, Glaucoma, Glioblastoma, High palate, Hirschsprung disease, Hydrocephalus, Hypoplasia of the maxilla, Hypospadias, Laryngomalacia, Lateral sclerosis, Legg-calve-perthes disease, Leukemia, Liver carcinoma, Lung carcinoma, Lung adenocarcinoma, Lymphoma, Non-hodgkin lymphoma, Lymphoblastic leukemia, Medulloblastoma, Melanoma, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microstomia, Mirror movements, Multicystic renal dysplasia, Multiple congenital anomalies, Myeloid leukemia with t(8;16)(p11;p13) translocation, Papillary cystadenoma of the epididymis, Parietal foramina, Patent ductus arteriosus, Polydactyly, Primary tethered cord syndrome, Proptosis, Prostatic neoplasms, Prostate cancer, Ptosis, Renal glomerular disease, Rubinstein-taybi syndrome, Scoliosis, Sezary syndrome, Sleep apnea, Spina bifida, Spina bifida occulta, Stereotyped behavior, Strawberry nevus of skin, Syndactyly, Syndactyly of the toes, Synophrys, Bladder carcinoma, Vascular ring, Ventricular septal defectView all (69 more) |
|
373
|
|
|
CAMP responsive element binding protein like 2 |
- |
|
|
374
|
|
|
CAMP responsive element modulator |
CREM-2, ICER, hCREM-2 |
Ankylosing spondylitis, Arthritis, Cholangitis, Crohn disease, Dermatitis, Diabetic cardiomyopathy, Inflammatory bowel disease, Juvenile arthritis, Myocardial infarction, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Psoriasis, Still disease, Ulcerative colitis |
|
375
|
|
|
Corticotropin releasing hormone |
CRF, CRH1 |
Alopecia, Alopecia, male pattern, Alzheimer disease, Androgenetic alopecia, Anhedonia, Anorexia, Anxiety disorder, Bipolar disorder, Clonic seizures, Cognitive disorder, Cryptogenic west syndrome, Cushing`s syndrome, Dysthymic disorder, Grand mal status epilepticus, Hypotonic seizures, Jackknife seizures, Jacksonian seizure, Melancholia, Mental depression, Mood disorder, Movement disorders, Neuroretinitis, Nocturnal epilepsy, Nonconvulsive status epilepticus, Petit mal status, Pituitary apoplexy, Pseudopelade, Psychomotor disorders, Retinitis, Salaam seizures, Schizophrenia, Seizure, Senile dementia, Spasmus nutans, Status epilepticus, Status marmoratus, Symptomatic west syndrome, West syndromeView all (23 more) |
|
376
|
|
|
Corticotropin releasing hormone binding protein |
CRF-BP, CRFBP |
|
|
377
|
|
|
Corticotropin releasing hormone receptor 1 |
CRF-R, CRF-R-1, CRF-R1, CRF1, CRFR-1, CRFR1, CRH-R-1, CRH-R1, CRHR, CRHR1L |
Alopecia, male pattern, Anhedonia, Anorexia, Anxiety disorder, Bipolar disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Dermatitis, Involutional depression, Involutional paraphrenia, Marfan syndrome, Mental depression, Mood disorder, Nonorganic psychosis, Osteoarthritis of hip, Parkinson disease, PsychosisView all (3 more) |
|
378
|
|
|
Corticotropin releasing hormone receptor 2 |
CRF-RB, CRF2, CRFR2, HM-CRF |
|
|
379
|
|
|
CRK proto-oncogene, adaptor protein |
CRKII, p38 |
|
|
380
|
|
|
CRK like proto-oncogene, adaptor protein |
- |
Ankyloglossia, Aortic aneurysm, Aortic valve insufficiency, Arachnodactyly, Atrial septal defect, Attention deficit hyperactivity disorder, Blepharophimosis, Bowel incontinence, Camptodactyly of fingers, Choanal atresia, Chromosome 22q11.2 deletion syndrome, Conotruncal anomaly face syndrome, Developmental delay, Digeorge syndrome, Distal 22q11.2 microdeletion syndrome, Dwarfism, Fistula of branchial cleft, Tourette syndrome, Hearing loss, Immunologic deficiency syndromes, Language disorders, Mental depression, Mental retardation, Microcephaly, Microstomia, Neoplasms, Obsessive-compulsive disorder, Oculomotor apraxia, Oculovestibuloauditory syndrome, Persistent truncus arteriosus, Shprintzen syndrome, Syndactyly of the toes, Ventricular septal defectView all (18 more) |
