Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal abnormality
|
| gptkbp:alsoKnownAs |
13q deletion
|
| gptkbp:associatedWith |
gptkb:retinoblastoma
chronic lymphocytic leukemia developmental delay congenital anomalies growth retardation mental retardation |
| gptkbp:chromosomeAffected |
gptkb:chromosome_13
|
| gptkbp:cytogeneticNotation |
gptkb:del(13q)
|
| gptkbp:frequencyInCLL |
most common cytogenetic abnormality in CLL
|
| gptkbp:geneticTesting |
gptkb:FISH
karyotyping array CGH |
| https://www.w3.org/2000/01/rdf-schema#label |
del(13q)
|
| gptkbp:inheritance |
usually de novo
|
| gptkbp:prognosisInCLL |
favorable
|
| gptkbp:bfsParent |
gptkb:small_lymphocytic_lymphoma
|
| gptkbp:bfsLayer |
6
|