2931
|
|
|
CROCC pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
2932
|
|
|
CROCC pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|
2933
|
|
|
Carnitine O-octanoyltransferase |
COT |
Curated: Lung cancer, Squamous cell carcinoma
Unreviewed: Anaplastic Lymphoma, Hypertension, Lung carcinoma, Non-Alcoholic Fatty Liver Disease, Obesity, Ovarian neoplasm, Papillary thyroid carcinoma, Paranoia, Prostatic neoplasm, Stroke
|
2934
|
|
|
C-reactive protein |
PTX1 |
Curated: Antiphospholipid syndrome, Anxiety disorder, Arthritis, Rheumatoid arthritis, Atherosclerosis, Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Cardiovascular disease, Cerebrovascular disorder, Ischemic heart disease, Obstructive airway disease, Congestive heart failure, Coronary artery disease, Crohn disease, Depression, Diabetes mellitus type 1, Diabetic retinopathy, Age-related macular degeneration, Heart disease, Heart failure, Hyperparathyroidism, Hypertension, Hypertriglyceridemia, Inflammatory bowel disease, Kidney failure, Lung cancer, Lung neoplasms, Systemic lupus erythematosus, Lupus nephritis, Macular degeneration, Major depressive disorder, Metabolic syndrome, Kawasaki disease, Myocardial ischemia, Obesity, Periodontitis, Psoriasis, Chronic obstructive pulmonary disease, Schizophrenia, Sleep apnea, Squamous cell carcinoma, Stevens-johnson syndrome, Substance abuse, Thrombosis
Unreviewed: N/A
|
2935
|
|
|
C-reactive protein pseudogene 1 |
- |
Curated: N/A
Unreviewed: Hypertension
|
2936
|
|
|
CDP-L-ribitol pyrophosphorylase A |
ISPD, LGMDR20, MDDGA7, MDDGC7, Nip, hISPD |
Curated: Androgenetic alopecia, Astrocytoma, Limb girdle muscular dystrophy, Carpal tunnel syndrome, Obstructive pulmonary disease, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Dry eye syndrome, Eye abnormalities, Huntington disease, Hydrocephalus, Osteonecrosis of the femoral head, Metabolic syndrome, Muscle eye brain disease, Muscular dystrophy, Myopathy, Ocular hypertension, Stroke, Diabetes mellitus type 2, Walker-warburg syndrome, myopathy caused by variation in CRPPA
Unreviewed: Absence Of Septum Pellucidum, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Agyria, alpha-Dystroglycanopathy, Amyotrophy, Anemia, Anterior segment dysgenesis, Aqueductal Stenosis, Bradyarrhythmia, Brain disease, Cardiovascular Abnormalities, Cataract, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebrovascular trauma, Cobblestone Lissencephaly, Communicating Hydrocephalus, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Hydrocephalus, Congenital Hypoplasia Of Penis, Congenital kyphoscoliosis, Congenital Muscular Dystrophy Without Intellectual Disability, Congenital Muscular Dystrophy-Dystroglycanopathy With Brain And Eye Anomalies, Cryptorchidism, Dandy-Walker Syndrome, Developmental Delay, Fetal Cerebral Ventriculomegaly, Frontal bossing, Fukuyama Type Congenital Muscular Dystrophy, Glaucoma, Hydrocephalus Ex-Vacuo, Hypoplasia Of Corpus Callosum, Hypoplasia Of The Optic Nerve, Hypotonia, Limb-girdle muscle atrophy, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy-Dystroglycanopathy, Macrocephaly, Macroglossia, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Microtia, Motor delay, Muscle Eye Brain Disease, Muscular Dystrophy, Congenital, Muscular Dystrophy-Dystroglycanopathy, Neural Tube Defect, Neuronal Heterotopia, Obstructive Hydrocephalus, Optic Atrophy, Pachygyria, Partial Agenesis Of Corpus Callosum, Persistent Hyperplastic Primary Vitreous, Polymicrogyria, Posteriorly Rotated Ear, Renal Carcinoma, Renal cell carcinoma, Retinal Detachment, Retinal Dysplasia, Retinal Dystrophy, Specific Learning Disorder, Submucosal cleft palate, Syndromic microphthalmia, Walker-Warburg Congenital Muscular Dystrophy, Walker-Warburg Syndrome
|
2937
|
|
|
CRPPA antisense RNA 1 |
ISPD-AS1 |
Curated: N/A
Unreviewed: Congenital Muscular Dystrophy-Dystroglycanopathy With Brain And Eye Anomalies, Limb-Girdle Muscular Dystrophy-Dystroglycanopathy, Muscular Dystrophy-Dystroglycanopathy
|
2938
|
|
|
- |
CRS3 |
Curated: N/A
Unreviewed: Neoplasms, Ovarian Epithelial carcinoma, Periodontitis
|
2939
|
|
|
Cofactor required for Sp1 transcriptional activation subunit 5 |
CRSP85 |
Curated: N/A
Unreviewed: N/A
|
2940
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|