Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | skeletal anomalies |
| gptkb:1p36_region | brain malformations |
| gptkb:1p36_region | gptkb:diabetes_mellitus |
| gptkb:1p36_region | distinct facial features |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | hypotonia |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:1p36_region | developmental delay |
| gptkb:9p21 | gptkb:bladder_cancer |
| gptkb:1p36_region | gptkb:intellectual_disability |
| gptkb:1p36_region | motor delay |
| gptkb:1p36_region | gptkb:autism_spectrum_disorder |
| gptkb:Prader-Willi_syndrome_critical_region | gptkb:Prader-Willi_syndrome |
| gptkb:1p36_region | epilepsy |
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:chromosome_9p21 | gptkb:leukemia |
| gptkb:1p36_region | seizures |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |