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 1476 - 1500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0014175 Endometriosis CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0678222 Breast Carcinoma CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0023487 Acute Promyelocytic Leukemia CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0026266 Mitral Valve Insufficiency CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0432272 Van Buchem disease CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0011854 Diabetes Mellitus, Insulin-Dependent CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0158761 Radioulnar Synostosis CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0019270 Hernia CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0030409 Paracoccidioidomycosis CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0016522 Foramen Ovale, Patent CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0036341 Schizophrenia CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0008497 Choriocarcinoma CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C2745959 Spondyloepiphyseal dysplasia, congenita CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0206686 Adrenocortical carcinoma CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0175778 Larsen syndrome CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0085083 Ovarian Hyperstimulation Syndrome CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0028754 Obesity CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0002418 Amblyopia CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0221356 Brachycephaly CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0036391 Schwartz-Jampel Syndrome CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0011849 Diabetes Mellitus CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C4551479 Schwartz-Jampel Syndrome, Type 1 CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0878544 Cardiomyopathies CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C0018818 Ventricular Septal Defects CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8
C3203102 Idiopathic pulmonary arterial hypertension CHST3 9469 carbohydrate sulfotransferase 3 Q7LGC8

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Last updated: August 19, 2024