Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | motor delay |
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | gptkb:cardiomyopathy |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | epilepsy |
| gptkb:1p36_region | hypothyroidism |
| gptkb:9p21 | gptkb:leukemia |
| gptkb:1p36_region | congenital heart defects |
| gptkb:1p36_region | hearing impairment |
| gptkb:1p36_region | autistic features |
| gptkb:Prader-Willi_syndrome_critical_region | gptkb:Prader-Willi_syndrome |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:1p36_region | speech delay |
| gptkb:1p36_region | seizures |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:1p36_region | vision impairment |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | renal anomalies |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |