DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 54301 - 54325 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C1621958 Glioblastoma Multiforme CANX 821 calnexin P27824
C0270911 Charcot-Marie-Tooth Disease, Type Ia (disorder) CANX 821 calnexin P27824
C0278510 Childhood Medulloblastoma CANX 821 calnexin P27824
C0410538 Pseudoachondroplasia CANX 821 calnexin P27824
C0026847 Spinal Muscular Atrophy CANX 821 calnexin P27824
C0206062 Lung Diseases, Interstitial CANX 821 calnexin P27824
C0162283 Nephrogenic Diabetes Insipidus CANX 821 calnexin P27824
C0024198 Lyme Disease CANX 821 calnexin P27824
C0279671 Cervical Squamous Cell Carcinoma CANX 821 calnexin P27824
C0029463 Osteosarcoma CANX 821 calnexin P27824
C0020459 Hyperinsulinism CANX 821 calnexin P27824
C0026705 Mucopolysaccharidosis II CANX 821 calnexin P27824
C0035334 Retinitis Pigmentosa CANX 821 calnexin P27824
C0042974 von Willebrand Disease CANX 821 calnexin P27824
C0038436 Post-Traumatic Stress Disorder CANX 821 calnexin P27824
C0699791 Stomach Carcinoma CANX 821 calnexin P27824
C2239176 Liver carcinoma CANX 821 calnexin P27824
C0086543 Cataract CALR3 125972 calreticulin 3 Q96L12
C0878544 Cardiomyopathies CALR3 125972 calreticulin 3 Q96L12
C0007194 Hypertrophic Cardiomyopathy CALR3 125972 calreticulin 3 Q96L12
C0042900 Vitiligo CALR3 125972 calreticulin 3 Q96L12
C3495498 Cardiomyopathy, Familial Hypertrophic, 1 (disorder) CALR3 125972 calreticulin 3 Q96L12
C1306459 Primary malignant neoplasm CALR 811 calreticulin P27797
C0040028 Thrombocythemia, Essential CALR 811 calreticulin P27797
C0029172 Oral Submucous Fibrosis CALR 811 calreticulin P27797

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Last updated: August 19, 2024