WormBase Tree Display for DO_term: DOID:0111781
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| DOID:0111781 | Name | Waisman syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that has_material_basis_in hemizygous or homozygous mutation in the RAB39B gene on chromosome Xq28. | ||||
| Synonym | Exact | Laxova-Opitz syndrome | |||
| early-onset parkinsonism-intellectual disability syndrome | |||||
| Parent | Is_a | DOID:225 | |||
| DOID:0080012 | |||||
| DB_info | Database | OMIM | disease | 311510 | |
| Attribute_of | Gene_by_orthology | WBGene00004286 |
