|
901
|
|
|
CCAAT enhancer binding protein alpha |
C/EBP-alpha, CEBP |
Acute myeloid leukemia, Alveolitis, Carcinoma, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Leukemia, Liver carcinoma, Head and neck cancer, Monocytic leukemia, Myeloblastic leukemia, Myelodysplastic syndrome, Myeloid leukemia, Myeloid leukemia with cebpa somatic mutations, Myeloid leukemia with t(8;21)(q22;q22) translocation, Neck neoplasms, Obesity, Promyelocytic leukemia, Pulmonary fibrosis, Radiation-induced cancer, Skin cancer, Skin neoplasms, Subfertility, Upper aerodigestive tract neoplasmsView all (10 more) |
|
902
|
|
|
Ssemaphorin 4F |
M-SEMA, PRO2353, S4F, SEMAM, SEMAW, m-Sema-M |
|
|
903
|
|
|
Semaphorin 4B |
SEMAC, SemC |
|
|
904
|
|
|
CCAAT enhancer binding protein beta |
C/EBP-beta, IL6DBP, NF-IL6, TCF5 |
|
|
905
|
|
|
Semaphorin 3C |
SEMAE, SemE |
|
|
906
|
|
|
MYB binding protein 1a |
P160, PAP2, Pol5 |
|
|
907
|
|
|
Fibulin 5 |
ADCL2, ARCL1A, ARMD3, CMT1H, DANCE, EVEC, FIBL-5, HNARMD, UP50 |
Age-related macular degeneration, Aortic aneurysm, Arachnodactyly, Bladder diverticulum, Bowel diverticulosis, Congenital diaphragmatic hernia, Congenital exomphalos, Congenital pectus excavatum, Congenital pes cavus, Congestive heart failure, Cutis laxa, Distal amyotrophy, Diverticulum of renal calyx, Drusen, Fibromuscular dysplasia, Heart failure, Hereditary sensorimotor neuropathy with hyperelastic skin, Hypothyroidism, Ileus, Lung diseases, Microcephaly, Myocardial infarction, Neuropathy, hereditary, with or without macular degeneration, Osteoporosis, Peripheral axonal neuropathy, Prostatic neoplasms, Prostate cancer, Ptosis, Pulmonary stenosis, Respiratory distress syndrome, Respiratory failure, Scoliosis, Supravalvar aortic stenosis, Vascular diseases, Vesicoureteral refluxView all (20 more) |
|
908
|
|
|
Calcium and integrin binding family member 2 |
DFNB48, KIP2, USH1J |
Anxiety disorder, Cataract, Cerebral cortical atrophy, Deafness, Developmental delay, Disorder of eye, Hallucinations, Hearing loss, Hemianopsia, Mental depression, Mental retardation, Motor delay, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Nyctalopia, Rod-cone dystrophy, Schizophrenia, Subcortical cerebral atrophy, Usher syndromeView all (4 more) |
|
909
|
|
|
Calcium and integrin binding 1 |
CIB, CIBP, EV3, KIP1, PRKDCIP, SIP2-28 |
|
|
910
|
|
|
CCAAT enhancer binding protein delta |
C/EBP-delta, CELF, CRP3, NF-IL6-beta |
|
