hypomyelinating leukodystrophy 2

Summary
Synonym
  • HLD2
  • PMLD1
  • Pelizaeus-Merzbacher-like disease 1
  • Pelizaeus-Merzbacher-like disease due to GJC2 mutation
Definition
A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of nystagmus, impaired motor development, ataxia, choreoathetotic movements, dysarthria, and progressive spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the GJC2 gene on chromosome 1q42.
Super Class
autosomal recessive disease hypomyelinating leukodystrophy
Disease Ontology
DOID:0060787
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
57165 GJC2 gap junction protein gamma 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: December 9, 2024