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Leukodystrophy, Hypomyelinating, 5 MeSH Supplementary Concept Data 2025


MeSH Supplementary
Leukodystrophy, Hypomyelinating, 5
Unique ID
C567166
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567166
Entry Term(s)
Hypomyelination And Congenital Cataract
Registry Numbers
0
Heading Mapped to
Cataract / congenital
*Hereditary Central Nervous System Demyelinating Diseases
Frequency
6
Note
mutation on hyccin (FAM126A)
Date of Entry
2012/11/05
Revision Date
2013/10/24
Leukodystrophy, Hypomyelinating, 5 Preferred
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