NF1 Microdeletion Syndrome MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: NF1 Microdeletion Syndrome
Unique ID: C563524
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563524
Registry Number: 0
Heading Mapped to: *Chromosome Deletion; Chromosomes, Human, Pair 17; *Learning Disabilities; *Intellectual Disability; *Neurofibromatoses; *Craniofacial Abnormalities
Frequency: 8
Date of Entry: 2012/11/05

NF1 Microdeletion Syndrome Preferred

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