1021
|
|
|
Coiled-coil domain containing 28B |
LTAP2B |
Asthma, Astigmatism, Atresia of vagina, Bardet-biedl syndrome, Brachydactyly, Cataract, Ciliopathies, Developmental delay, Diabetes mellitus, Glaucoma, High palate, Hypertension, Hypodontia, Hypogonadism, Left ventricular hypertrophy, Liver fibrosis, Macrocephaly, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrogenic diabetes insipidus, Nystagmus, Obesity, Penis agenesis, Polydactyly of toes, Retinal dystrophy, Rod-cone dystrophy, Specific learning disorder, Speech disorders, Strabismus, Syndactyly, Talipes transversoplanus, Postaxial hand polydactylyView all (18 more) |
1022
|
|
|
Centromere protein O |
CENP-O, ICEN-36, MCM21R |
|
1023
|
|
|
Calbindin 1 |
CALB, D-28K |
|
1024
|
|
|
Calbindin 2 |
CAB29, CAL2, CR |
|
1025
|
|
|
Cytochrome b-245 chaperone 1 |
C17orf62, CGD5, Eros |
|
1026
|
|
|
Cell division cycle 73 |
C1orf28, FIHP, HPTJT, HRPT1, HRPT2, HYX |
Chondrocalcinosis, Cortical adenoma of kidney, Dysphagia, Endocrine gland cancer, Endometriosis, Fibroma, Hamartoma, Head and neck carcinoma, Head and neck neoplasms, Hypercalcemia, Hyperparathyroidism, Hyperparathyroidism-jaw tumor syndrome, Lipoma, Head and neck cancer, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Ossifying fibroma of the jaw, Osteopenia, Osteoporosis, Pancreatic adenocarcinoma, Pancreatitis, Papillary renal carcinoma, Parathyroid adenoma, Parathyroid gland adenocarcinoma, Parathyroid carcinoma, Parathyroid neoplasms, Peptic ulcer, Phosphate diabetes, Polycystic kidney disease, Renal cyst, Renal insufficiency, Testicular neoplasms, Thyroid carcinoma, Thyroid gland oncocytic adenoma, Uterine fibroidsView all (21 more) |
1027
|
|
|
Coronin 7 |
0610011B16Rik, CRN7, POD1 |
|
1028
|
|
|
Cysteinyl-tRNA synthetase 2, mitochondrial |
COXPD27, cysRS |
Autism, Cerebellar hypoplasia, Cerebral atrophy, Combined oxidative phosphorylation deficiency, Developmental delay, Developmental regression, Dysphagia, Epileptic encephalopathy, Hydrops fetalis, Hypoplasia of corpus callosum, Hypoplastic hippocampus, Mental retardation, Myoclonic seizures, Status epilepticus |
1029
|
|
|
Centrosomal protein 97 |
2810403B08Rik, LRRIQ2 |
|
1030
|
|
|
Calcitonin related polypeptide alpha |
CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT, KC, PCT |
Abdominal migraine, Alveolitis, Arthritis, Autism, Bronchial hyperreactivity, Catalepsy, Common migraine, Confusional migraine, Down syndrome, Hemicrania migraine, Hypercalcemia, Hypertension, Mental retardation, Lesion of sciatic nerve, Migraine, Milk-alkali syndrome, Osteoarthrosis deformans, Prostatic neoplasms, Prostate cancer, Pulmonary fibrosis, Sciatic nerve neuralgia-neuritis, Sciatic nerve palsy, Sciatic neuritis, Sciatic neuropathy, Status migrainosus, Trigeminal neuralgia, Trisomy 21View all (12 more) |