Charcot-Marie-Tooth disease type 4B1

Summary
Synonym
  • CMT4B1
  • Charcot-Marie-Tooth neuropathy type 4B1
  • autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1
Definition
A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding the myotubularin-related protein-2 (MTMR2).
Super Class
Charcot-Marie-Tooth disease type 4 autosomal recessive disease
External Links
Disease Ontology
DOID:0110191
Mondo Disease Ontology
MeSH
ORDO
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
The Human Phenotype Ontology
Displaying entries 11 - 13 of 13 in total
HPO ID HPO Term
HP:0010628 Facial palsy
HP:0002650 Scoliosis
HP:0003701 Proximal muscle weakness
Displaying 1 entry
Gene ID Gene Symbol Description
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