Microcephaly with Chorioretinopathy, Autosomal Dominant MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Microcephaly with Chorioretinopathy, Autosomal Dominant
Unique ID: C563583
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563583
Registry Numbers: 0
Heading Mapped to: *Microcephaly; *Retinal Diseases
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Microcephaly with Chorioretinopathy, Autosomal Dominant Preferred

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