Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | vision problems |
| gptkb:9p21 | gptkb:bladder_cancer |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | hearing impairment |
| gptkb:Angelman_syndrome_critical_region | Prader-Willi syndrome (if paternal) |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:1p36_region | obesity |
| gptkb:1p36_region | hypotonia |
| gptkb:1p36_region | distinct facial features |
| gptkb:1p36_region | cognitive impairment |
| gptkb:1p36_region | gptkb:cardiomyopathy |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |
| gptkb:1p36_region | behavioral problems |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:1p36_region | orofacial clefts |
| gptkb:1p36_region | gptkb:intellectual_disability |
| gptkb:1p36_region | renal anomalies |
| gptkb:1p36_region | growth delay |
| gptkb:9p21 | gptkb:glioblastoma |