WormBase Tree Display for DO_term: DOID:0060363
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| DOID:0060363 | Name | glycerol kinase deficiency | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An inherited metabolic disorder characterized_by wide range of phenotypic variability; patients can have severe metabolic and CNS abnormalities, while others possess hyperglycerolemia and glyceroluria with no other apparent phenotype and that has_material_basis_in mutation in the GK gene on chromosome Xp21. | ||||
| Parent | Is_a | DOID:655 | |||
| DB_info | Database | OMIM | disease | 307030 | |
| Attribute_of | Gene_by_orthology | WBGene00020007 |
