MeSH Browser

MeSH Supplementary: Heterotopia, Periventricular, Autosomal Recessive
Unique ID: C564292
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564292
Entry Term(s): Periventricular Heterotopia with Microcephaly, Autosomal Recessive; Periventricular Nodular Heterotopia 2
Registry Number: 0
Heading Mapped to: *Periventricular Nodular Heterotopia
Frequency: 0
Note: mutation in ARFGEF2
Date of Entry: 2012/11/05

Heterotopia, Periventricular, Autosomal Recessive MeSH Supplementary Concept Data 2024