|
1331
|
|
|
Cell division cycle 6 |
CDC18L, HsCDC18, HsCDC6, MGORS5 |
Camptodactyly of fingers, Clinodactyly, Breast aplasia, Anotia, Mandibular aplasia, Congenital hypoplasia of penis, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Ear diseases, Ear-patella-short stature syndrome, Epispadias, Gastroesophageal reflux disease, Hypertrophy of clitoris, Hypoplasia of the maxilla, Hypospadias, Liver carcinoma, Meier-gorlin syndrome, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Motor delay, Myeloproliferative disorder, Sclerocystic ovaries, Penis agenesis, Polycystic ovary syndrome, Posteriorly rotated ear, Respiratory failure, Seckel syndrome, Specific learning disorder, Submucosal cleft palateView all (19 more) |
|
1332
|
|
|
Cell division cycle 20 |
CDC20A, OOMD14, OZEMA14, bA276H19.3, p55CDC |
|
|
1333
|
|
|
Cell division cycle 25B |
MPIP2 |
|
|
1334
|
|
|
Cell division cycle 25C |
CDC25, PPP1R60 |
|
|
1335
|
|
|
Cell division cycle 27 |
ANAPC3, APC3, CDC27Hs, D0S1430E, D17S978E, H-NUC, HNUC, NUC2 |
|
|
1336
|
|
|
Copper chaperone for superoxide dismutase |
- |
|
|
1337
|
|
|
Cell division cycle 42 |
CDC42Hs, G25K, TKS |
Adrenal cancer, Adrenal neoplasia, Anaplastic carcinoma, Carcinoma, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral cortical atrophy, Clinodactyly, Congenital camptodactyly, Cryptorchidism, Developmental delay, Dysmorphic features, Endometriosis, Exotropia, Hearing loss, Heart septal defects, Hydronephrosis, Hypoplasia of corpus callosum, Hypospadias, Immunologic deficiency syndromes, Macrostomia, Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome, Mental retardation, Multiple congenital anomalies, Neck webbing, Nevus, Oculomotor nerve palsy, Optic atrophy, Patent ductus arteriosus, Platelet-type bleeding disorder, Posteriorly rotated ear, Ptosis, Pulmonary stenosis, Renal aplasia, Schizophrenia, Scoliosis, Strabismus, Synophrys, Takenouchi-kosaki syndrome, Uterine fibroids, Plexiform leiomyomaView all (26 more) |
|
1338
|
|
|
Cadherin 1 |
Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM, UVO |
Adenocarcinoma, Anaplastic carcinoma, Benign neoplasm of stomach, Urinary bladder cancer, Bladder neoplasm, Blepharocheilodontic syndrome, Breast cancer, Invasive duct and lobular carcinoma, Mammary neoplasms, Breast carcinoma, Hereditary cancer syndrome, Carcinoma, Cleft palate and bilateral cleft lip, Clinodactyly, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital euryblepharon, Ductal carcinoma, Dysgerminoma, Endometrial neoplasms, Endometrial carcinoma, Gastric cancer, Gastritis, Hearing loss, Hereditary breast cancer, Hereditary nonpolyposis colorectal cancer, Hypodontia, Hypoplasia of the maxilla, Imperforate anus, Malignant melanoma of skin, Malnutrition, Marfan syndrome, Melanoma, Mesothelioma, Nasopharyngeal carcinoma, Neural tube defect, Oropharyngeal dysphagia, Otitis media, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Ovarian papillary adenocarcinoma, Pancreatic neoplasm, Pancreatic cancer, Peg-shaped teeth, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Salivary gland neoplasm, Malignant neoplasm of salivary gland, Stomach neoplasms, Stomach carcinoma, Syndactyly of fingers, Thyroid carcinoma, Ulcerative colitis, Velopharyngeal insufficiencyView all (43 more) |
