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1011
|
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C-X-C motif chemokine receptor 4 |
CD184, D2S201E, FB22, HM89, HSY3RR, LAP-3, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM, WHIMS, WHIMS1 |
Arthritis, Breast cancer, Mammary neoplasms, Breast carcinoma, Bronchiectasis, Cervical cancer, Congenital neutropenia, Juvenile arthritis, Lymphadenitis, Lymphopenia, Marfan syndrome, Melanoma, Myelokathexis, Nephrosclerosis, Neutropenia, Otitis media, Parotitis, Periodontitis, Pharyngitis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Rheumatoid arthritis, Sinusitis, Speech disorders, Still disease, Tetralogy of fallot, VitiligoView all (12 more) |
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1012
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CRELD disulfide isomerase 1 |
AVSD2, CIRRIN, JELANS |
Aortic coarctation, Aortic valve sclerosis, Atrioventricular septal defect, partial, with heterotaxy syndrome, Bicuspid aortic valve, Ciliopathies, Complete atrioventricular septal defect with ventricular hypoplasia, Complete atrioventricular septal defect-tetralogy of fallot, Congenital atresia of pulmonary artery, Dextrocardia, Double outlet right ventricle, Heterotaxia, Hypoplastic left heart syndrome, Partial atrioventricular canal defect, Partial defect of atrioventricular canal, Patent ductus arteriosus, Pulmonary venous return anomaly, Situs ambiguus, Tetralogy of fallot, Transient ischemic attackView all (4 more) |
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1013
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Collectin subfamily member 11 |
3MC2, CL-11, CL-K1-I, CL-K1-II, CL-K1-IIa, CL-K1-IIb, CLK1 |
3mc syndrome, Accessory nipple, Blepharophimosis, Congenital exomphalos, Craniofacial ulnar renal syndrome, Craniosynostosis, Cryptorchidism, Developmental delay, Incontinentia pigmenti achromians, Malpuech facial clefting syndrome, Mental retardation, Oral cleft, Pigmentation disorders, Ptosis, Radioulnar synostosis, Scoliosis, Spina bifida occulta, StrabismusView all (3 more) |
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1014
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Cell cycle regulator of NHEJ |
C7orf49, CYREN-1, CYREN-2, MRI, MRI-2 |
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1015
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Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase |
CDG1Z, DEE50, EIEE50, GATD4 |
Abetalipoproteinemia, Anemia, Beta thalassemia, Brain atrophy, Cerebral atrophy, Colorectal cancer, Congenital disorder of glycosylation, Congenital hypoplastic anemia, Cooley`s anemia, Developmental delay, Developmental regression, Epileptic encephalopathy, Erythroblastic leukemia, Hemoglobinopathy, Hereditary spherocytosis, Status epilepticus, ThalassemiaView all (2 more) |
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1016
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CUE domain containing 2 |
C10orf66, bA18I14.5 |
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1017
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CaM kinase like vesicle associated |
1G5, VACAMKL |
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1018
|
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Centromere protein M |
C22orf18, CENP-M, PANE1 |
|
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1019
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Coiled-coil domain containing 86 |
Cgr1 |
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1020
|
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Caspase recruitment domain family member 14 |
BIMP2, CARMA2, PRP, PSORS2, PSS1 |
Autoinflammatory disease, Eczema, Exfoliative dermatitis, Hyperkeratosis, Ichthyosis, Moyamoya disease, Neoplasms, Palmoplantar keratoderma, Palmoplantar pustules, Parakeratosis, Psoriasiform eczema, Psoriasis, Subungual hyperkeratosis |
