Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:chromosome_15q11-q13 | Prader-Willi syndrome (paternal) |
| gptkb:1p36_region | vision problems |
| gptkb:1p36_region | developmental delay |
| gptkb:1p36_region | hearing loss |
| gptkb:1p36_region | hypotonia |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:1p36_region | autistic features |
| gptkb:1p36_region | orofacial clefts |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:1p36_region | motor delay |
| gptkb:1p36_region | brain malformations |
| gptkb:22q13.33 | gptkb:Phelan-McDermid_syndrome |
| gptkb:chromosome_15q11-q13 | Angelman syndrome (maternal) |
| gptkb:chromosome_22q13.31 | gptkb:autism_spectrum_disorder |
| gptkb:Prader-Willi/Angelman_region | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:1p36_region | behavioral problems |
| gptkb:1p36_region | vision impairment |
| gptkb:1p36_region | congenital heart defects |
| gptkb:chromosome_22q13.31 | gptkb:intellectual_disability |
| gptkb:1p36_region | gptkb:intellectual_disability |