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 11101 - 11125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0020678 Hypotrichosis XYLT1 64131 xylosyltransferase 1 Q86Y38
C0025958 Microcephaly XYLT1 64131 xylosyltransferase 1 Q86Y38
C0013170 Drug habituation XYLT1 64131 xylosyltransferase 1 Q86Y38
C1857941 Brooke-Spiegler syndrome XYLT1 64131 xylosyltransferase 1 Q86Y38
C0023467 Leukemia, Myelocytic, Acute XYLT1 64131 xylosyltransferase 1 Q86Y38
C0029422 Osteochondrodysplasias XYLT1 64131 xylosyltransferase 1 Q86Y38
C1510472 Drug Dependence XYLT1 64131 xylosyltransferase 1 Q86Y38
C0158761 Radioulnar Synostosis XYLT1 64131 xylosyltransferase 1 Q86Y38
C0004114 Astrocytoma XYLT1 64131 xylosyltransferase 1 Q86Y38
C1565489 Renal Insufficiency XYLT1 64131 xylosyltransferase 1 Q86Y38
C0376359 Gronblad-Strandberg Syndrome XYLT1 64131 xylosyltransferase 1 Q86Y38
C0017601 Glaucoma XYLT1 64131 xylosyltransferase 1 Q86Y38
C0271561 Somatotropin deficiency XYLT1 64131 xylosyltransferase 1 Q86Y38
C0013336 Dwarfism XYLT1 64131 xylosyltransferase 1 Q86Y38
C0005129 Bernard-Soulier Syndrome XYLT1 64131 xylosyltransferase 1 Q86Y38
C0544755 Genu varum XYLT1 64131 xylosyltransferase 1 Q86Y38
C0027092 Myopia XYLT1 64131 xylosyltransferase 1 Q86Y38
C0026269 Mitral Valve Stenosis XYLT1 64131 xylosyltransferase 1 Q86Y38
C0016202 Flatfoot XYLT1 64131 xylosyltransferase 1 Q86Y38
C0019572 Hirsutism XYLT1 64131 xylosyltransferase 1 Q86Y38
C0029408 Degenerative polyarthritis XYLT1 64131 xylosyltransferase 1 Q86Y38
C0026277 Mixed Salivary Gland Tumor XYLT1 64131 xylosyltransferase 1 Q86Y38
C0020608 Hypodontia XYLT1 64131 xylosyltransferase 1 Q86Y38
C0007196 Restrictive cardiomyopathy XYLT1 64131 xylosyltransferase 1 Q86Y38
C0015300 Exophthalmos XYLT1 64131 xylosyltransferase 1 Q86Y38

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Last updated: August 19, 2024