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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
|---|---|---|---|---|---|
| C1561643 | Chronic Kidney Diseases | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0268731 | Renal glomerular disease | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C4225306 | CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0020295 | Hydronephrosis | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0205700 | Asymmetric Septal Hypertrophy | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0700095 | Central neuroblastoma | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0029882 | Otitis Media | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0086647 | Mucopolysaccharidosis Type IIIA | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0027651 | Neoplasms | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0022658 | Kidney Diseases | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0270707 | Kluver-Bucy Syndrome | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0001418 | Adenocarcinoma | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0033578 | Prostatic Neoplasms | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0003850 | Arteriosclerosis | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0086651 | Mucopolysaccharidosis, MPS-IV-A | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0011265 | Presenile dementia | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0086650 | MPS III D | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0003615 | Appendicitis | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0036857 | Severe intellectual disability | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C1704321 | Nephrotic Syndrome, Minimal Change | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0019572 | Hirsutism | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0018801 | Heart failure | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0029422 | Osteochondrodysplasias | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0028860 | Oculocerebrorenal Syndrome | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
| C0497327 | Dementia | NAGLU | 4669 | N-acetyl-alpha-glucosaminidase | P54802 |
