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Microcephaly, Primary Autosomal Recessive, 5 MeSH Supplementary Concept Data 2023


MeSH Supplementary
Microcephaly, Primary Autosomal Recessive, 5
Unique ID
C563871
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563871
Registry Number
0
Heading Mapped to
*Microcephaly
Frequency
2
Note
mutation in ASPM
Date of Entry
2012/11/05
Microcephaly, Primary Autosomal Recessive, 5 Preferred
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