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loading...| Preferred Name |
Philadelphia Chromosome [Disease/Finding] |
|
| Synonyms |
Philadelphia Chromosome Ph1 Chromosome Ph 1 Chromosome |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002391 |
|
| altLabel |
Philadelphia Chromosome Ph1 Chromosome Ph 1 Chromosome |
|
| cui |
C0031526 |
|
| MESH DEFINITION |
An aberrant form of human CHROMOSOME 22 characterized by translocation of the distal end of chromosome 9 from 9q34, to the long arm of chromosome 22 at 22q11. It is present in the bone marrow cells of 80 to 90 per cent of patients with chronic myelocytic leukemia (LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE). |
|
| MESH DUI |
D010677 |
|
| MeSH name |
Philadelphia Chromosome |
|
| MESH UI |
M0016591 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000002391 |
|
| NUI |
N0000002391 |
|
| prefLabel |
Philadelphia Chromosome [Disease/Finding] |
|
| tui |
T046 |
|
| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MSHFRE/D010677 | MSHFRE | CUI | |
| http://purl.bioontology.org/ontology/CSP/1259-6116 | CRISP | CUI | |
| http://purl.bioontology.org/ontology/MESH/D010677 | MESH | CUI |