Chromosome 8p11 myeloproliferative syndrome

Preferred Label : Chromosome 8p11 myeloproliferative syndrome;

CISMeF acronym : SCLL;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Stem cell leukemia/lymphoma; SCLL;

Description : The 8p11 myeloproliferative syndrome is a rare aggressive condition characterized in its typical form by the occurrence, either simultaneously or sequentially, of a BCR/ABL-negative myeloproliferative disorder and a lymphoma, usually a precursor T-lymphoblastic lymphoma. The disease most often terminates in acute myeloid leukemia (Goradia et al., 2008).;

Prefixed ID : #613523;

Détails

Origin ID

613523;

UMLS CUI

C3150773;

Automatic exact mappings (from CISMeF team)
- ZMYM2 wt Allele [NCIt concept]
False automatic mappings
- Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement [ORDO Disease]
ORDO concept(s)
- Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality (disorder) [SNOMED CT concept]
- Myeloid-lymphoid neoplasm with FGFR1 rearrangement (morphologic abnormality) [SNOMED CT concept]
- Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement [NCIt concept]

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

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