hypomyelinating leukodystrophy 19

Summary
Synonym
  • HLD19
Definition
A hypomyelinating leukodystrophy characterized by onset of transient neurologic abnormalities in early infancy with resolution within the first or second decades that has_material_basis_in heterozygous mutation in the TMEM63A gene on chromosome 1q42.
Super Class
autosomal dominant disease hypomyelinating leukodystrophy
External Links
Disease Ontology
DOID:0070400
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9725 TMEM63A transmembrane protein 63A
Displaying 1 entry
Gene ID Gene Symbol Description Source
208795 Tmem63a transmembrane protein 63a
Displaying 1 entry
Gene ID Gene Symbol Description Source
850942 CSC1 Csc1p

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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