Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:9p21 | mesothelioma |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:1p36_region | hearing impairment |
| gptkb:1p36_region | microcephaly |
| gptkb:chromosome_17p11.2 | Smith-Magenis syndrome |
| gptkb:1p36_region | renal anomalies |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:9p21 | gptkb:leukemia |
| gptkb:1p36_region | hearing loss |
| gptkb:1p36_region | gptkb:intellectual_disability |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:chromosome_9p21 | gptkb:familial_melanoma |
| gptkb:1p36_region | feeding difficulties |
| gptkb:1p36_region | seizures |
| gptkb:Prader-Willi_syndrome_critical_region | gptkb:Prader-Willi_syndrome |
| gptkb:Prader-Willi_syndrome_region | gptkb:Prader-Willi_syndrome |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | autistic features |