WormBase Tree Display for DO_term: DOID:0060395
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| DOID:0060395 | Name | chromosome 15q24 deletion syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15. | ||||
| Synonym | Exact | 15q24 microdeletion syndrome | |||
| Parent | Is_a | DOID:0050736 | |||
| DOID:0060388 | |||||
| DB_info | Database | OMIM | disease | 613406 | |
| Attribute_of | Gene_by_orthology | WBGene00004117 |
