Chromosome Xp21 Deletion Syndrome
Disease ID: disease_node_17096
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| Dbxref | ICD10CM:Q99.8, MIM:300679, ORDO:261476 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID |
| Synonyms | Xp21 microdeletion syndrome, complex glycerol kinase deficiency, monosomy Xp21 |
| Doid Label | chromosome Xp21 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region. |
| Disease Node Id | disease_node_17096 |
| Doid Id | DOID_0060427 |
| Label | Chromosome Xp21 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)