Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | vision problems |
| gptkb:chromosome_13q14 | hematological malignancies |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:1p36_region | gptkb:autism_spectrum_disorder |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | distinct facial features |
| gptkb:1p36_region | skeletal anomalies |
| gptkb:Angelman_syndrome_critical_region | Prader-Willi syndrome (if paternal) |
| gptkb:chromosome_17p11.2 | Smith-Magenis syndrome |
| gptkb:chromosome_9p21 | gptkb:leukemia |
| gptkb:1p36_region | hypothyroidism |
| gptkb:15q11-q13 | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:9p21 | pancreatic cancer |
| gptkb:Prader-Willi_syndrome_critical_region | gptkb:Prader-Willi_syndrome |
| gptkb:1p36_region | cognitive impairment |
| gptkb:1p36_region | gptkb:intellectual_disability |
| gptkb:9p21 | gptkb:bladder_cancer |
| gptkb:1p36_region | growth delay |