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Leukodystrophy, Hypomyelinating, 4 MeSH Supplementary Concept Data 2022


MeSH Supplementary
Leukodystrophy, Hypomyelinating, 4
Unique ID
C567390
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567390
Entry Term(s)
Mitochondrial Hsp60 Chaperonopathy
Registry Number
0
Heading Mapped to
*Hereditary Central Nervous System Demyelinating Diseases
*Mitochondrial Diseases
Frequency
8
Note
mutation in HSPD1
Date of Entry
2012/11/05
Leukodystrophy, Hypomyelinating, 4 Preferred
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