MeSH Browser

MeSH Supplementary: Silengo Lerone Pelizza syndrome
Unique ID: C537336
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537336
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; Bone and Bones / abnormalities; *Microcephaly; Optic Atrophy / congenital; *Brain Diseases, Metabolic, Inborn
Frequency: 0
Note: Microcephaly, schizencephaly, decorticated disturbance of the neurological function, congenital optic atrophy and nystagmus
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Silengo Lerone Pelizza syndrome MeSH Supplementary Concept Data 2025