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 43551 - 43575 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0270820 Gelastic Epilepsy NGLY1 55768 N-glycanase 1 Q96IV0
C0027066 Myoclonus NGLY1 55768 N-glycanase 1 Q96IV0
C1531647 Cerebral ventriculomegaly NGLY1 55768 N-glycanase 1 Q96IV0
C0027651 Neoplasms NGLY1 55768 N-glycanase 1 Q96IV0
C0010038 Corneal Opacity NGLY1 55768 N-glycanase 1 Q96IV0
C0442874 Neuropathy NGLY1 55768 N-glycanase 1 Q96IV0
C0025202 melanoma NGLY1 55768 N-glycanase 1 Q96IV0
C0010043 Corneal Ulcer NGLY1 55768 N-glycanase 1 Q96IV0
C0699791 Stomach Carcinoma NGLY1 55768 N-glycanase 1 Q96IV0
C0029456 Osteoporosis NGLY1 55768 N-glycanase 1 Q96IV0
C0006826 Malignant Neoplasms NGLY1 55768 N-glycanase 1 Q96IV0
C0029124 Optic Atrophy NGLY1 55768 N-glycanase 1 Q96IV0
C0017154 Gastritis, Atrophic NGLY1 55768 N-glycanase 1 Q96IV0
C1306459 Primary malignant neoplasm NGLY1 55768 N-glycanase 1 Q96IV0
C0035334 Retinitis Pigmentosa NGLY1 55768 N-glycanase 1 Q96IV0
C4316812 Fibrinogen Deficiency NGLY1 55768 N-glycanase 1 Q96IV0
C0152025 Polyneuropathy NGLY1 55768 N-glycanase 1 Q96IV0
C0271270 Oculovestibuloauditory syndrome NGLY1 55768 N-glycanase 1 Q96IV0
C0085109 Corneal Neovascularization NGLY1 55768 N-glycanase 1 Q96IV0
C0036439 Scoliosis, unspecified NGLY1 55768 N-glycanase 1 Q96IV0
C0038379 Strabismus NGLY1 55768 N-glycanase 1 Q96IV0
C0015310 Exotropia NGLY1 55768 N-glycanase 1 Q96IV0
C0005745 Blepharoptosis NGLY1 55768 N-glycanase 1 Q96IV0
C0221356 Brachycephaly NGLY1 55768 N-glycanase 1 Q96IV0
C0520679 Sleep Apnea, Obstructive NGLY1 55768 N-glycanase 1 Q96IV0

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Last updated: August 19, 2024