Microcephaly, Primary Autosomal Recessive, 5 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Microcephaly, Primary Autosomal Recessive, 5
Unique ID: C563871
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563871
Registry Numbers: 0
Heading Mapped to: *Microcephaly
Frequency: 2
Note: mutation in ASPM
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Microcephaly, Primary Autosomal Recessive, 5 Preferred

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