Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
81 to 90 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

81
C1q and TNF related 5
CTRP5, MFRP
Macular degeneration, Microphthalmia, Microphthalmia with retinitis pigmentosa and ocular anomalies, Nanophthalmos, Optic atrophy, Retinitis pigmentosa

82
C1q and TNF related 6
CTFP6, CTRP6, ZACRP6
Autoimmune disease, Autoimmune thyroid disease, Breast cancer, Diabetes mellitus type 1, Graves disease, Hypothyroidism, Systemic lupus erythematosus, Thyroid disease, Diabetes mellitus type 2, Vitiligo

83
C1q and TNF related 7
CTRP7, ZACRP7
Bell's palsy, Conduct disorder, Diverticular disease

84
C1q and TNF related 8
CTRP8, UNQ5829
Osteoarthritis

85
Complement C1r
EDS8, EDSPD1
Systemic lupus erythematosus, Complement pathway abnormality, Vascular dementia, Ehlers-danlos syndrome, Endometriosis, Periodontal ehlers-danlos syndrome

86
Complement C1r subcomponent like
C1RL1, C1RLP, C1r-LP, CLSPa
Ehlers-danlos syndrome

87
Complement C1s
EDSPD2
Alzheimer disease, Ankylosing spondylitis, Autoimmune hepatitis, Autoimmune disease, Complement pathway abnormality, Complement component deficiency, Coronary artery disease, Ehlers-danlos syndrome, Hashimoto disease, Hereditary angioedema, Lung cancer, Periodontal ehlers-danlos syndrome

88
Complement C2
ARMD14, CO2
Alzheimer disease, Atrophic macular degeneration, Autism, C1 esterase inhibitor deficiency, Cancer, Interstitial cystitis, Complement pathway abnormality, Complement component deficiency, Coronary artery disease, Irritant dermatitis, Dermatomyositis, Endometriosis, Glaucoma, Hepatocellular carcinoma, Hypertension
View all (17 more)

89
Chromosome 20 open reading frame 202
-
Multiple sclerosis, Oligodendroglioma

90
Chromosome 20 open reading frame 203
-
Cardiovascular disease, Hypertension, Insomnia, Willis-ekbom disease, Diabetes mellitus type 2