thrombocytopenia chromosome breakage

Preferred Label : thrombocytopenia chromosome breakage;

MeSH note : Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage;

MeSH synonym : thrombocytopenia, autosomal dominant; helmerhorst heaton crossen syndrome; thrombocytopenia 2; thrombocytopenia, autosomal dominant, 2;

Details

Origin ID

C536519;

UMLS CUI

C1861185;

Currated CISMeF NLP mapping
- Thrombocytopenia 2 [NCIt concept]
- Thrombocytopenia 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosome breakage [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- thrombocytopenia [MeSH Descriptor]
Record concept(s)
- Thrombocytopenia chromosome breakage [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Thrombocytopenia 2 [OMIM Phenotype]
- Thrombocytopenia 2 [NCIt concept]

Keyword's position in hierarchy(ies) :

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