Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | vision problems |
| gptkb:1p36_region | congenital heart defects |
| gptkb:1p36_region | developmental delay |
| gptkb:1p36_region | microcephaly |
| gptkb:1p36_region | growth delay |
| gptkb:1p36_region | vision impairment |
| gptkb:1p36_region | hearing impairment |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | hearing loss |
| gptkb:1p36_region | brain malformations |
| gptkb:22q13.33 | gptkb:Phelan-McDermid_syndrome |
| gptkb:chromosome_17p11.2 | Smith-Magenis syndrome |
| gptkb:1p36_region | gptkb:autism_spectrum_disorder |
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:Prader-Willi_syndrome_region | gptkb:Prader-Willi_syndrome |
| gptkb:17p11.1 | Smith-Magenis syndrome |
| gptkb:1p36_region | skeletal anomalies |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:1p36_region | gptkb:intellectual_disability |