Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | behavioral problems |
| gptkb:chromosome_9p21 | leukemia |
| gptkb:1p36_region | microcephaly |
| gptkb:CFHR3 | protection against age-related macular degeneration |
| gptkb:1p36_region | developmental delay |
| gptkb:1p36_region | vision impairment |
| gptkb:17p11.1 | Smith-Magenis syndrome |
| gptkb:1p36_region | epilepsy |
| gptkb:1p36_region | distinct facial features |
| gptkb:Angelman_syndrome_critical_region | Prader-Willi syndrome (if paternal) |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:1p36_region | cardiomyopathy |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | orofacial clefts |
| gptkb:1p36_region | speech delay |
| gptkb:chromosome_22q13.31 | intellectual disability |
| gptkb:15q11-q13 | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:1p36_region | obesity |
| gptkb:1p36_region | autistic features |
| gptkb:9p21 | mesothelioma |