MeSH Browser

MeSH Supplementary: Thrombocytopenia Robin sequence
Unique ID: C536898
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536898
Entry Term(s): Braddock Carey syndrome
Registry Numbers: 0
Heading Mapped to: *Growth Disorders; *Pierre Robin Syndrome; Thrombocytopenia / congenital; *Facies; *Agenesis of Corpus Callosum
Frequency: 5
Note: Congenital thrombocytopenia, Robin sequence, agenesis of the corpus callosum, distinctive facies and developmental delay
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Thrombocytopenia Robin sequence MeSH Supplementary Concept Data 2025