MeSH Browser

MeSH Supplementary: Thrombocytopenia chromosome breakage
Unique ID: C536519
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536519
Entry Term(s): Helmerhorst Heaton Crossen syndrome; Thrombocytopenia 2; Thrombocytopenia, Autosomal Dominant, 2; Thrombocytopenia, autosomal dominant
Registry Number: 0
Heading Mapped to: Thrombocytopenia / *congenital; *Chromosome Breakage; *Chromosome Disorders
Frequency: 18
Note: Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Thrombocytopenia chromosome breakage MeSH Supplementary Concept Data 2023