|
521
|
|
|
Cytochrome P450 family 19 subfamily A member 1 |
ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM |
Acanthosis nigricans, Adenocarcinoma, Ambiguous genitalia, Aromatase deficiency, Aromatase excess syndrome, Autism, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cirrhosis, Cryptorchidism, Diabetes mellitus, Dwarfism, Endometrial carcinoma, Endometrioma, Endometriosis, Enlarged polycystic ovaries, Esophagus neoplasm, Fatty liver, Female pseudohermaphroditism, Genital infantilism, Gynecomastia, Hyperlipidemia, Hypogonadism, Hypogonadotropic hypogonadism, Hypopituitarism, Marfan syndrome, Obesity, Osteopenia, Osteoporosis, Sclerocystic ovaries, Ovarian cysts, Ovarian diseases, Physiologic amenorrhea, Polycystic ovary syndrome, Prostatic neoplasms, Prostate cancer, Sexual infantilism, Sheehan syndrome, SubfertilityView all (26 more) |
|
522
|
|
|
Cytochrome P450 family 21 subfamily A member 2 |
CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B |
Adrenal hyperplasia, Adrenogenital syndrome, Autoimmune thyroiditis, Complement component deficiency, Congenital adrenal hyperplasia, Coronary artery disease, Coronary heart disease, Development disorder, Diabetes, Diabetes mellitus, Endometriosis, Exudative macular degeneration, Geographic atrophy, Graves disease, Gynecomastia, Hydrops fetalis, Hyperandrogenism, Hypertension, Hypoglycemia, Hypospadias, Lipomucopolysaccharidosis, Liver carcinoma, Lung adenocarcinoma, Lung cancer, Lung carcinoma, Lupus erythematosus, Age-related macular degeneration, Melanoma, Membranous glomerulonephritis, Mental depression, Movement disorders, Mucolipidosis, Multiple congenital anomalies, Multiple sclerosis, Myasthenia gravis, Non-classic congenital adrenal hyperplasia, Non-obstructive azoospermia, Oral ulcer, Pemphigus vulgaris, Biliary cirrhosis, Psoriatic arthritis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Scleroderma, Sialidase deficiency, Skin carcinoma, Takayasu arteritis, Trichohepatoenteric syndrome, Ulcerative colitis, VitiligoView all (36 more) |
|
523
|
|
|
Cytochrome P450 family 24 subfamily A member 1 |
CP24, CYP24, HCAI, HCINF1, P450-CC24 |
Aortic valve sclerosis, Breast cancer, Mammary neoplasms, Breast carcinoma, Calcium metabolism disorders, Hypercalcemia, Kidney failure, Lung neoplasms, Lung cancer, Marfan syndrome, Mental retardation, Milk-alkali syndrome, Miscarriage, Nephrocalcinosis, Nephrolithiasis, Osteoporosis, Pulmonary stenosis, Renal insufficiencyView all (3 more) |
|
524
|
|
|
Cytochrome P450 family 26 subfamily A member 1 |
CP26, CYP26, P450RAI, P450RAI1 |
|
|
525
|
|
|
Cytochrome P450 family 27 subfamily A member 1 |
CP27, CTX, CYP27 |
Atherosclerosis, Cataract, Cerebellar atrophy, Cerebral atrophy, Cerebrotendinous xanthomatosis, Cholelithiasis, Cholestasis, Congenital cataract, Delusions, Dementia, Developmental delay, Developmental regression, Disorder of eye, Distal lower limb amyotrophy, Dysphagia, Eyelid xanthoma, Hallucinations, Hypercholesterolemia, Liver cirrhosis, Liver fibrosis, Malabsorption syndrome, Mental depression, Mental retardation, Metabolic bone disorder, Myocardial infarction, Nephrolithiasis, Nervous system diseases, Osteopenia, Osteoporosis, Pseudobulbar palsy, Retinitis pigmentosa, Sensory neuropathy, Spastic tetraparesis, Speech disorders, Tuberous xanthoma, Vitamin d deficiency, Xanthoma, Xanthoma tendinosum, Cholestanol storage diseaseView all (24 more) |
|
526
|
|
|
Cytochrome P450 family 27 subfamily B member 1 |
CP2B, CYP1, CYP1alpha, CYP27B, P450c1, PDDR, VDD1, VDDR, VDDRI, VDR |
Dental enamel hypoplasia, Dwarfism, Frontal bossing, Hypercalcemia, Hyperparathyroidism, Hypocalcemic seizures, Hypocalcemic vitamin d-dependent rickets, Milk-alkali syndrome, Motor delay, Multiple sclerosis, Polymyositis, Polymyositis ossificans, Rachitic rosary, Rickets, Vitamin d-dependent rickets |
|
527
|
|
|
Cytochrome P450 family 51 subfamily A member 1 |
CP51, CYP51, CYPL1, LDM, P450-14DM, P450L1 |
|
|
528
|
|
|
Chromosome 11 open reading frame 65 |
MFI |
Adrenocortical adenoma, Nonmedullary thyroid carcinoma, Ataxia telangiectasia, Ataxia-telangiectasia syndrome, Breast cancer, Mammary neoplasms, Breast carcinoma, Hereditary cancer syndrome, Carcinoma, Cerebellar ataxia, Colorectal cancer, Glioblastoma, Glioma, Hereditary breast and ovarian cancer syndrome, Immunologic deficiency syndromes, Islet cell tumor, Lipoma, Lymphoid leukemia, Malignant lymphoma, lymphocytic, intermediate differentiation, Malignant melanoma of skin, Melanoma, Movement disorders, Ductal carcinoma, Osteoma, Ovarian neoplasm, Paraganglioma, Sarcoma, T-cell prolymphocytic leukemia, Uterine fibroids, Plexiform leiomyomaView all (15 more) |
|
529
|
|
|
C-type lectin domain family 12 member A |
CD371, CLL-1, CLL1, DCAL-2, MICL, hKLRL1 |
|
|
530
|
|
|
C-type lectin like 1 |
CLECL1P, DCAL-1, DCAL1 |
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