Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | vision impairment |
| gptkb:1p36_region | obesity |
| gptkb:1p36_region | cognitive impairment |
| gptkb:1p36_region | hypothyroidism |
| gptkb:13q14_(RB1_gene) | loss of tumor suppressor function |
| gptkb:1p36_region | epilepsy |
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:Angelman_syndrome_critical_region | gptkb:Angelman_syndrome |
| gptkb:chromosome_17p11.2 | Smith-Magenis syndrome |
| gptkb:1p36_region | microcephaly |
| gptkb:1p36_region | gptkb:diabetes_mellitus |
| gptkb:1p36_region | hearing impairment |
| gptkb:1p36_region | distinct facial features |
| gptkb:1p36_region | renal anomalies |
| gptkb:9p21 | gptkb:leukemia |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | gptkb:cardiomyopathy |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |
| gptkb:CFHR3 | protection against age-related macular degeneration |