Jacobsen Distal 11Q Deletion Syndrome
Disease ID: disease_node_11980
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| Dbxref | GARD:307, MESH:D054868, MIM:147791, ORDO:2308 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID, MESH |
| Synonyms | Jacobsen distal 11q deletion syndrome, chromosome 11q deletion syndrome, partial 11q monosomy syndrome |
| Mesh Id | D054868 |
| Mesh Label | Jacobsen Distal 11q Deletion Syndrome |
| Mesh Subclassof | D013921, D025063 |
| Doid Label | Jacobsen Syndrome |
| Doid Description | A chromosomal deletion syndrome that is characterized by growth retardation, psychomotor retardation, distinctive facial features, skeletal abnormalities, and isoimmune thrombocytopenia that has_material_basis_in deletion of terminal chromosome 11q. |
| Disease Node Id | disease_node_11980 |
| Doid Id | DOID_0111723 |
| Label | Jacobsen Distal 11Q Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)