|
661
|
|
|
Chromosome 17 open reading frame 58 |
- |
|
|
662
|
|
|
Caveolae associated protein 1 |
CAVIN, CGL4, FKSG13, PTRF, cavin-1 |
Acanthosis nigricans, Atherosclerosis, Atrial fibrillation, Breast cancer, Cirrhosis, Congenital lipodystrophy, Congestive heart failure, Crohn disease, Diabetes mellitus, Dysphagia, Eczema, Fatty liver, Hyperinsulinism, Hypertrophic cardiomyopathy, Ileus, Immunologic deficiency syndromes, Isolated somatotropin deficiency, Kidney disease, Lipoatrophic diabetes mellitus, Lipoatrophy, Lipodystrophy, Liver failure, Malocclusion, Mental retardation, Muscular dystrophy, Myocardial infarction, Myopathy, Nervous system diseases, Osteopenia, Osteoporosis, Pancreatitis, Polycystic ovary syndrome, Precocious puberty, Psoriasis, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Scoliosis, Secondary physiologic amenorrhea, Somatotropin deficiency, Talipes transversoplanus, Ventricular hypertrophyView all (27 more) |
|
663
|
|
|
Chromosome 1 open reading frame 167 |
- |
|
|
664
|
|
|
Chromosome 1 open reading frame 185 |
- |
|
|
665
|
|
|
Cytochrome b561 family member D1 |
- |
|
|
666
|
|
|
Coiled-coil domain containing 141 |
CAMDI |
Breast hypoplasia, Cryptorchidism, Dysarthria, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mirror movements, Nystagmus, Obesity, Osteochondrodysplasia, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Skeletal dysplasiaView all (4 more) |
|
667
|
|
|
CYP1B1 antisense RNA 1 |
C2orf58 |
|
|
668
|
|
|
Chromosome 3 open reading frame 38 |
- |
|
|
669
|
|
|
Coiled-coil domain containing 66 |
- |
|
|
670
|
|
|
Cytochrome P450 family 4 subfamily V member 2 |
BCD, CYP4AH1 |
|
