platelet disorder, familial, with associated myeloid malignancy

Preferred Label : platelet disorder, familial, with associated myeloid malignancy;

MeSH synonym : thrombocytopenia, familial, with propensity to acute myelogenous leukemia; platelet disorder, Aspirin-Like; FPDAML; FPDMM;

Détails

Origin ID

C563324;

UMLS CUI

C1832388;

Currated CISMeF NLP mapping
- Familial Platelet Disorder with Associated Myeloid Malignancy [NCIt concept]
- Familial platelet disorder with associated myeloid malignancy [ORDO Disease]
- Familial platelet syndrome with predisposition to acute myelogenous leukaemia [ICD-11 More detail]
- Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder) [SNOMED CT concept]
- Platelet disorder, familial, with associated myeloid malignancy [OMIM Phenotype]
MeSH term(s) associated for indexing
- blood coagulation disorders, inherited [MeSH Descriptor]
- blood platelet disorders [MeSH Descriptor]
- leukemia, myeloid, acute [MeSH Descriptor]
Record concept(s)
- platelet disorder, familial, with associated myeloid malignancy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Platelet Disorder with Associated Myeloid Malignancy [NCIt concept]
- Familial platelet disorder with associated myeloid malignancy [ORDO Disease]
- Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder) [SNOMED CT concept]
- Platelet disorder, familial, with associated myeloid malignancy [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

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