Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:chromosome_9p21 | gptkb:familial_melanoma |
| gptkb:1p36_region | brain malformations |
| gptkb:Angelman_syndrome_critical_region | Prader-Willi syndrome (if paternal) |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:Prader-Willi_syndrome_region | gptkb:Prader-Willi_syndrome |
| gptkb:Angelman_syndrome_critical_region | gptkb:Angelman_syndrome |
| gptkb:1p36_region | speech delay |
| gptkb:chromosome_7q22 | hematological malignancies |
| gptkb:1p36_region | hearing loss |
| gptkb:1p36_region | developmental delay |
| gptkb:1p36_region | skeletal anomalies |
| gptkb:chromosome_13q14 | hematological malignancies |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:DLEU1 | 13q14 deletion syndrome |
| gptkb:1p36_region | hearing impairment |
| gptkb:1p36_region | vision problems |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:1p36_region | epilepsy |
| gptkb:chromosome_22q13.31 | gptkb:autism_spectrum_disorder |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |