Charcot-Marie-Tooth disease type 4C

Summary
Synonym
  • CMT4C
  • Charcot-Marie-Tooth neuropathy type 4C
  • autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C
Definition
A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SH3TC2 gene.
Super Class
Charcot-Marie-Tooth disease type 4 autosomal recessive disease
External Links
Disease Ontology
DOID:0110183
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 29 in total
Gene ID Gene Symbol Description Source
4051 CYP4F3 cytochrome P450 family 4 subfamily F member 3
4099 MAG myelin associated glycoprotein
4534 MTM1 myotubularin 1
5230 PGK1 phosphoglycerate kinase 1
5236 PGM1 phosphoglucomutase 1
5332 PLCB4 phospholipase C beta 4
5621 PRNP prion protein (Kanno blood group)
5631 PRPS1 phosphoribosyl pyrophosphate synthetase 1
5743 PTGS2 prostaglandin-endoperoxide synthase 2
8898 MTMR2 myotubularin related protein 2

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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