Partial Trisomy 1q

Preferred Label : Partial Trisomy 1q;

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]
- Early/Prefibrotic Primary Myelofibrosis [NCIt concept]
- Overt Primary Myelofibrosis [NCIt concept]
- Primary Myelofibrosis [NCIt concept]
- Recurrent Primary Myelofibrosis [NCIt concept]
- Refractory Primary Myelofibrosis [NCIt concept]