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
External Links
Disease Ontology
DOID:0060787
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
2629 GBA1 glucosylceramidase beta 1
5297 PI4KA phosphatidylinositol 4-kinase alpha
Related Glycoprotein

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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