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Standards Ontologies Notations
myotonic disease

Summary
Definition
A muscular dystrophy that is characterized by progressive muscle wasting and weakness.
Super Class
muscular dystrophy
External Links
Disease Ontology
DOID:450
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
7903 ST8SIA4 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4
23236 PLCB1 phospholipase C beta 1
26033 ATRNL1 attractin like 1
159371 SLC35G1 solute carrier family 35 member G1
Related Glycoprotein
Displaying entry 11 - 11 of 11 in total
UniProt ID Protein Name Source
Q9NQ66 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024