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Microcephaly with Chorioretinopathy, Autosomal Recessive MeSH Supplementary Concept Data 2024


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