MeSH Browser

MeSH Supplementary: Ataxia-Microcephaly-Cataract Syndrome
Unique ID: C563086
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563086
Entry Term(s): AMC Syndrome
Registry Numbers: 0
Heading Mapped to: *Ataxia; *Cataract; *Microcephaly; *Eye Diseases, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Ataxia-Microcephaly-Cataract Syndrome MeSH Supplementary Concept Data 2025