|
981
|
|
|
Complement C8 alpha chain |
- |
|
|
982
|
|
|
Complement C8 beta chain |
C82 |
|
|
983
|
|
|
Complement C8 gamma chain |
C8C |
|
|
984
|
|
|
Complement C9 |
ARMD15, C9D |
Antibody deficiency syndrome, C9 deficiency, Complement component deficiency, Dermatomyositis, Diabetes, Diabetes mellitus, Exudative macular degeneration, Facial dermatosis, Favre-racouchot syndrome, Geographic atrophy, Immunodeficiency, Immunologic deficiency syndromes, Kidney disease, Kidney failure, Leukemia, Liver carcinoma, Age-related macular degeneration, Malignant mesothelioma, Nodular elastosis with cysts and comedones, Pancreatic carcinoma, Pancreatic cancerView all (6 more) |
|
985
|
|
|
Collagen type XIV alpha 1 chain |
UND |
|
|
986
|
|
|
Clarin 1 |
RP61, USH3, USH3A |
Anxiety disorder, Astigmatism, Cataract, Ciliopathies, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hallucinations, Hearing loss, Hemianopsia, Hyperinsulinism, Hypogonadism, Keratoconus, Mental depression, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Schizophrenia, Usher syndromeView all (10 more) |
|
987
|
|
|
CAP-Gly domain containing linker protein 2 |
CLIP, CLIP-115, CYLN2, WBSCR3, WBSCR4, WSCR3, WSCR4 |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Cholelithiasis, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Cryptorchidism, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple renal cysts, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Scoliosis, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (70 more) |
|
988
|
|
|
Cilia and flagella associated protein 410 |
C21orf2, LRRC76, RDMS, SMDAX, YF5/A2 |
Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Anxiety disorder, Asthenozoospermia, Cataract, Cone dystrophy, Cone-rod dystrophy, Dwarfism, Jeune thoracic dystrophy, Laryngospasm, Mental depression, Mood swings, Nyctalopia, Nystagmus, Optic atrophy, Respiratory failure, Retinal dystrophy, Retinal dystrophy with or without macular staphyloma, Retinitis pigmentosa, Rhizomelia, Rod-cone dystrophy, Spondylometaphyseal dysplasia, Strudwick syndrome, Thoracic hypoplasiaView all (9 more) |
|
989
|
|
|
CCHC-type zinc finger nucleic acid binding protein |
CNBP1, DM2, PROMM, RNF163, ZCCHC22, ZNF9 |
|
|
990
|
|
|
Carbonic anhydrase 1 |
CA-I, CAB, Car1, HEL-S-11 |
|
