Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | hearing loss |
| gptkb:chromosome_9p21 | gptkb:leukemia |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | hypothyroidism |
| gptkb:1p36_region | behavioral problems |
| gptkb:1p36_region | developmental delay |
| gptkb:9p21 | mesothelioma |
| gptkb:1p36_region | thyroid dysfunction |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |
| gptkb:Prader-Willi_syndrome_critical_region | gptkb:Prader-Willi_syndrome |
| gptkb:CFHR3 | protection against age-related macular degeneration |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:9p21 | pancreatic cancer |
| gptkb:1p36_region | epilepsy |
| gptkb:1p36_region | vision problems |
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | microcephaly |
| gptkb:1p36_region | gptkb:autism_spectrum_disorder |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | congenital heart defects |