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 |
---|---|---|---|---|---|
C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0020224 | Polyhydramnios | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0031117 | Peripheral Neuropathy | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0020545 | Hypertension, Renovascular | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0017572 | Gingival Recession | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0011581 | Depressive disorder | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C0000768 | Congenital Abnormality | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C4551902 | Craniosynostosis, Type 1 | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0795830 | CHROMOSOME 9p DELETION SYNDROME | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0265425 | 9p partial monosomy syndrome | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0010278 | Craniosynostosis | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0265233 | Cryptophthalmos syndrome | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C1619700 | RENAL ADYSPLASIA | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0242473 | Anus Prolapse | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0007222 | Cardiovascular Diseases | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C2931150 | Synostotic Anterior Plagiocephaly | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0015393 | Eye Abnormalities | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0311249 | Cryptophthalmos | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0265534 | Scaphycephaly | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0235833 | Congenital diaphragmatic hernia | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0019693 | HIV Infections | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0221356 | Brachycephaly | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0478099 | Other deletions of part of a chromosome | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0019284 | Diaphragmatic Hernia | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
C0026010 | Microphthalmos | FREM1 | 158326 | FRAS1 related extracellular matrix 1 | Q5H8C1 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024