Gardner Morrisson Abbot syndrome MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Gardner Morrisson Abbot syndrome
Unique ID: C535643
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535643
Entry Term(s): Thrombocytopenia multiple congenital anomaly
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Thrombocytopenia
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Gardner Morrisson Abbot syndrome Preferred

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