Spondyloocular Syndrome, Autosomal Recessive MeSH Supplementary Concept Data 2026

Details
Concepts

MeSH Supplementary: Spondyloocular Syndrome, Autosomal Recessive
Unique ID: C565285
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565285
Registry Numbers: 0
Heading Mapped to: *Cataract; *Osteochondrodysplasias; *Retinal Detachment; *Eye Diseases, Hereditary; *Craniofacial Abnormalities
Frequency: 4
Date Introduced: 2012/11/05
Last Updated: 2012/11/05

Spondyloocular Syndrome, Autosomal Recessive Preferred

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