MeSH Browser

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 Number: 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 MeSH Supplementary Concept Data 2024