Partial Trisomy 1q

Preferred Label : Partial Trisomy 1q;

NCIt definition : A chromosomal rearrangement characterized by the presence of three copies of genetic material derived from the long arm of chromosome 1 (1q).;

Details

Origin ID

C36521;

UMLS CUI

C4708596;

Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Trisomy 1q syndrome (disorder) [SNOMED CT concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Accelerated Phase Primary Myelofibrosis [NCIt concept]
- Blast Phase Primary Myelofibrosis [NCIt concept]
- Chronic Phase Primary Myelofibrosis [NCIt concept]
- Overt Primary Myelofibrosis [NCIt concept]
- Prefibrotic Primary Myelofibrosis [NCIt concept]
- Primary Myelofibrosis [NCIt concept]
- Primary Myelofibrosis with CALR Mutation [NCIt concept]
- Primary Myelofibrosis with JAK2 Mutation [NCIt concept]
- Primary Myelofibrosis with MPL Mutation [NCIt concept]
- Recurrent Primary Myelofibrosis [NCIt concept]
- Refractory Primary Myelofibrosis [NCIt concept]

Keyword's position in hierarchy(ies) :

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