Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:22q13.33 | gptkb:Phelan-McDermid_syndrome |
| gptkb:CFHR3 | protection against age-related macular degeneration |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | hearing impairment |
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | congenital heart defects |
| gptkb:1p36_region | renal anomalies |
| gptkb:1p36_region | gptkb:diabetes_mellitus |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:1p36_region | thyroid dysfunction |
| gptkb:1p36_region | vision problems |
| gptkb:17p11.1 | Smith-Magenis syndrome |
| gptkb:9p21 | pancreatic cancer |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:1p36_region | microcephaly |
| gptkb:1p36_region | orofacial clefts |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:9p21 | mesothelioma |
| gptkb:1p36_region | distinct facial features |