Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | intellectual disability |
| gptkb:1p36_region | hearing loss |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:17p11.1 | Smith-Magenis syndrome |
| gptkb:1p36_region | renal anomalies |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | developmental delay |
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:1p36_region | hearing impairment |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:15q11-q13 | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:1p36_region | distinct facial features |
| gptkb:chromosome_17p11.2 | Smith-Magenis syndrome |
| gptkb:chromosome_22q13.31 | gptkb:autism_spectrum_disorder |
| gptkb:1p36_region | brain malformations |
| gptkb:9p21 | leukemia |
| gptkb:1p36_region | epilepsy |
| gptkb:9p21 | pancreatic cancer |
| gptkb:Prader-Willi/Angelman_region | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:chromosome_9p21 | gptkb:familial_melanoma |