MeSH Browser

MeSH Supplementary: Microcephaly with Chorioretinopathy, Autosomal Recessive
Unique ID: C565379
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565379
Registry Numbers: 0
Heading Mapped to: *Microcephaly; *Retinal Diseases; *Eye Diseases, Hereditary; *Choroid Diseases
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Microcephaly with Chorioretinopathy, Autosomal Recessive MeSH Supplementary Concept Data 2025