Alternative names (2)
deletionAssociatedWith • deletionCausesRandom triples
| Subject | Object |
|---|---|
| gptkb:1p36_region | microcephaly |
| gptkb:1p36_region | obesity |
| gptkb:chromosome_13q14 | hematological malignancies |
| gptkb:1p36_region | developmental delay |
| gptkb:1p36_region | vision problems |
| gptkb:15q11-q13 | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:9p21 | gptkb:glioblastoma |
| gptkb:1p36_region | seizures |
| gptkb:15q11-q13 | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:1p36_region | speech delay |
| gptkb:1p36_region | behavioral abnormalities |
| gptkb:Prader-Willi/Angelman_region | gptkb:Prader-Willi_syndrome_(paternal_deletion) |
| gptkb:chromosome_9p21 | gptkb:familial_melanoma |
| gptkb:1p36_region | vision impairment |
| gptkb:1p36_region | motor delay |
| gptkb:Prader-Willi/Angelman_region | gptkb:Angelman_syndrome_(maternal_deletion) |
| gptkb:chromosome_13q14 | tumorigenesis |
| gptkb:chromosome_22q13.31 | gptkb:autism_spectrum_disorder |
| gptkb:1p36_region | craniofacial dysmorphism |
| gptkb:17p11.1 | Smith-Magenis syndrome |