Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | hypothyroidism |
| gptkb:1p36_region | epilepsy |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:1p36_region | obesity |
| gptkb:9p21 | gptkb:leukemia |
| gptkb:1p36_region | hypotonia |
| gptkb:1p36_region | orofacial clefts |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:1p36_region | hearing loss |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:22q13.33 | gptkb:Phelan-McDermid_syndrome |
| gptkb:chromosome_9p21 | gptkb:leukemia |
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:1p36_region | hearing impairment |
| gptkb:chromosome_9p21 | gptkb:familial_melanoma |
| gptkb:1p36_region | vision problems |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |
| gptkb:Angelman_syndrome_critical_region | Prader-Willi syndrome (if paternal) |
| gptkb:1p36_region | gptkb:cardiomyopathy |