Charcot-Marie-Tooth disease type 2Y

Summary
Synonym
  • CMT2 due to VCP mutation
  • CMT2Y
  • Charcot-Marie-Tooth neuropathy type 2Y
  • autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation
  • autosomal dominant axonal Charcot-Marie-Tooth type 2Y
Definition
A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the VCP gene on chromosome 9p13.
Super Class
Charcot-Marie-Tooth disease type 2 autosomal dominant disease
External Links
Disease Ontology
DOID:0110168
Mondo Disease Ontology
ORDO
OMIM
The Human Phenotype Ontology
Displaying entries 1 - 10 of 51 in total
HPO ID HPO Term
HP:0000708 Atypical behavior
HP:0000712 Emotional lability
HP:0000762 Decreased nerve conduction velocity
HP:0001260 Dysarthria
HP:0001288 Gait disturbance
HP:0001315 Reduced tendon reflexes
HP:0001761 Pes cavus
HP:0001765 Hammertoe
HP:0002094 Dyspnea
HP:0002136 Broad-based gait
Displaying 1 entry
Gene ID Gene Symbol Description
7415 VCP valosin containing protein

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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