General Information of Disease (ID: DISN15TG)

Disease Name Leukodystrophy, hypomyelinating, 16
Synonyms HLD16; leukodystrophy, hypomyelinating, 16
Disease Hierarchy
DISVY1TT: Leukodystrophy
DISN15TG: Leukodystrophy, hypomyelinating, 16
Disease Identifiers
MONDO ID
MONDO_0054791
UMLS CUI
C4693779
OMIM ID
617964
MedGen ID
1631337

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
TMEM106B OTUWA6NW Strong Autosomal dominant [1]
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References

1 The FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomes. EMBO J. 2014 Mar 3;33(5):450-67. doi: 10.1002/embj.201385857. Epub 2013 Dec 19.