Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2181 to 2190 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2181
Cadherin 5
7B4, CD144
Biliary cirrhosis, Breast neoplasms, Colorectal neoplasms, Liver cirrhosis, Mesothelioma, Biliary cholangitis

2182
Cadherin 6
CAD6, KCAD
Cachexia, Color vision deficiency, Insomnia, Large artery stroke, Major depressive disorder, Hypertension, Vascular dementia

2183
Cadherin 7
CDH7L1
Bipolar disorder, Colorectal neoplasms, Alzheimer disease, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Obesity, Ovarian cancer, Ovarian serous carcinoma, Retinal detachment, Scoliosis, Diabetes mellitus type 2, Depression

2184
Cadherin 8
Nbla04261
Attention deficit hyperactivity disorder, Autism, Breast cancer, Insomnia, Major depressive disorder, Mood disorder, Non-small cell lung carcinoma, Oligodendroglioma, Scoliosis, Substance abuse

2185
Cadherin 9
-
Autism, Dental caries, Laryngeal disease, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Pelvic organ prolapse, Diabetes mellitus type 2

2186
Cadherin related family member 1
CORD15, PCDH21, PRCAD, RP65
Cone dystrophy, Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Optic atrophy, Retinitis pigmentosa

2187
Cadherin related family member 3
CDH28
Alzheimer disease, Asthma, Atrial fibrillation, Crohn disease, Multiple sclerosis, Obesity

2188
Cadherin related family member 4
CDH29, PRO34300
Attention deficit hyperactivity disorder, Autism, Insomnia, Myocardial infarction

2189
Cadherin related family member 5
MLPCDH, MU-PCDH, MUCDHL, MUPCDH
Hypothyroidism, Systemic lupus erythematosus, Systemic sclerosis

2190
CDAN1 interacting nuclease 1
C15orf41, HH114
Alzheimer disease, Congenital dyserythropoietic anemia, Colorectal cancer, Gastroesophageal reflux disease, Willis-ekbom disease