Chromosome Xp11.3 Deletion Syndrome MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Chromosome Xp11.3 Deletion Syndrome
Unique ID: C564481
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564481
Entry Term(s): Mental Retardation, X-Linked, With Retinitis Pigmentosa
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa; *Mental Retardation, X-Linked
Frequency: 0
Date of Entry: 2012/11/05

Chromosome Xp11.3 Deletion Syndrome Preferred

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