WormBase Tree Display for DO_term: DOID:0111715
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| DOID:0111715 | Name | Schaaf-Yang syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome characterized by delayed psychomotor development, impaired intellectual development, hypotonia, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the maternally imprinted gene MAGEL2 on chromosome 15q11.2. | ||||
| Synonym | Exact | MAGEL2-related PWLS | |||
| MAGEL2-related Prader-Willi-like syndrome | |||||
| PWLS | |||||
| SHFYNG | |||||
| Parent | Is_a | DOID:225 | |||
| DB_info | Database | OMIM | disease | 615547 | |
| Attribute_of | Gene_by_orthology | WBGene00001579 |
