|
491
|
|
|
Cytochrome P450 family 1 subfamily A member 1 |
AHH, AHRR, CP11, CYP1, CYPIA1, P1-450, P450-C, P450DX |
Ankylosing spondylitis, Arterial occlusive disease, Arteritis, Psoriatic arthritis, Autism, Behcet disease, Bradycardia, Breast neoplasm, Bronchitis, Hepatocellular carcinoma, Cardiomegaly, Kidney disease, Obstructive airway disease, Congenital clubfoot, Contact dermatitis, Coronary artery disease, Cystic fibrosis, Allergic contact dermatitis, Atopic dermatitis, Diabetes mellitus, Experimental diabetes, Diabetes mellitus type 2, Gout, Graves disease, Hematuria, Hepatomegaly, Hyperoxia, Hypersensitivity, Hypertension, Hypospadias, Male infertility, Kidney failure, Kidney neoplasm, Long qt syndrome, Lung cancer, Systemic lupus erythematosus, Non-small cell lung carcinoma, Occupational disease, Parkinson disease, Periodontitis, Peripheral vascular disease, Polycystic ovary syndrome, Porphyria cutanea tarda, Prostatic neoplasm, Psoriasis, Chronic obstructive pulmonary disease, Sjogren syndrome, Squamous cell carcinoma, DepressionView all (34 more) |
|
492
|
|
|
Cytochrome P450 family 1 subfamily A member 2 |
CP12, CYPIA2, P3-450, P450(PA) |
Alzheimer disease, Atrophy, Autism, Hepatocellular carcinoma, Squamous cell carcinoma, Cardiovascular disease, Cholelithiasis, Kidney disease, Obstructive airway disease, Colorectal neoplasm, Coronary artery disease, Diabetes mellitus type 2, Gout, Growth disorder, Hepatomegaly, Hypertension, Kidney failure, Liver cirrhosis, Liver disease, Liver neoplasm, Lung cancer, Lung neoplasms, Methemoglobinemia, Neural tube defect, Nonalcoholic fatty liver disease, Non-small cell lung carcinoma, Osteoarthritis, Porphyria cutanea tarda, Chronic obstructive pulmonary disease, Schizophrenia, Splenic disease, SplenomegalyView all (17 more) |
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493
|
|
|
Coiled-coil domain containing 167 |
C6orf129, HSPC265 |
|
|
494
|
|
|
Cytochrome P450 family 1 subfamily B member 1 |
ASGD6, CP1B, CYPIB1, GLC3A, P4501B1 |
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Basal cell carcinoma, Breast neoplasm, Squamous cell carcinoma, Cardiomegaly, Asthma, Colorectal neoplasm, Congenital ocular coloboma, Contact dermatitis, Coronary artery disease, Melanoma, Fatty liver, Fatty liver, alcoholic, Glaucoma, Hepatomegaly, Primary congenital glaucoma, Keratinocyte carcinoma, Lung neoplasms, Mouth neoplasm, Non-melanoma skin carcinoma, Obesity, Ovarian neoplasm, Open angle glaucoma, Prostatic neoplasm, Respiratory system disease, Skin cancer, Skin neoplasm, DepressionView all (14 more) |
|
495
|
|
|
Cytochrome P450 family 2 subfamily A member 6 |
CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB |
Brain disease, Bronchus cancer, Large cell carcinoma, Small cell carcinoma, Chronic bronchitis, Lung disease, Obstructive pulmonary disease, Colorectal neoplasm, Esophageal squamous cell carcinoma, Hepatitis b, Hepatitis c, Liver disease, Lung cancer, Lung neoplasms, Nasopharyngeal carcinoma, Non-small cell lung carcinoma, Prostatic neoplasm, Respiratory system cancer, Squamous cell carcinoma, Stomach neoplasms, Upper aerodigestive tract neoplasmView all (6 more) |
|
496
|
|
|
Cytochrome P450 family 3 subfamily A member 7 |
CP37, CYPIIIA7, P-450(HFL33), P-450111A7, P450-HFLA, P450HLp2 |
|
|
497
|
|
|
Cytochrome P450 family 2 subfamily A member 13 |
CPAD, CYP2A, CYPIIA13 |
|
|
498
|
|
|
Cytochrome P450 family 2 subfamily B member 6 |
CPB6, CYP2B, CYP2B7, CYP2B7P, CYPIIB6, EFVM, IIB1, P450 |
Autism, Hepatocellular carcinoma, Cholelithiasis, Cutaneous mastocytosis, Gliosarcoma, Human immunodeficiency virus infection, Kidney failure, Mastocytosis, Non-organic psychosis, Psychotic disorders, Tuberculoma |
|
499
|
|
|
Cytochrome P450 family 2 subfamily C member 19 |
CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19 |
Sickle cell anemia, Atrial fibrillation, Autism, Cardiovascular disease, Major depressive disorder, Eosinophilia, Genetic predisposition to disease, Kidney failure, Depression, Migraine, Premature ovarian failure, Peptic ulcer disease, Prostatic neoplasm, Tuberculoma |
|
500
|
|
|
Cytochrome P450 family 2 subfamily C member 8 |
CPC8, CYP2C8DM, CYPIIC8, MP-12/MP-20 |
Autism, Hepatocellular carcinoma, Gout, Kidney disease, Kidney failure, Nervous system disease, Non-neoplastic peripheral nervous system disease, Osteonecrosis, Peripheral nervous system disease, Peripheral neuropathy, Renal hypertension, Rhabdomyolysis, Tuberculosis |