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Spondyloocular Syndrome, Autosomal Recessive MeSH Supplementary Concept Data 2022


MeSH Supplementary
Spondyloocular Syndrome, Autosomal Recessive
Unique ID
C565285
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565285
Entry Term(s)
Registry Number
0
Heading Mapped to
*Cataract
*Osteochondrodysplasias
*Retinal Detachment
*Eye Diseases, Hereditary
*Craniofacial Abnormalities
Frequency
4
Date of Entry
2012/11/05
Spondyloocular Syndrome, Autosomal Recessive Preferred
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