Trisomy 18 Syndrome
Disease ID: disease_node_262
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| Dbxref | ICD9CM:758.2, MESH:D000073842, NCI:C101362, SNOMEDCT_US_2023_03_01:51500006, UMLS_CUI:C0152096 |
|---|---|
| Subclassof | DOID_0060429 |
| Data Source | DOID, MESH |
| Synonyms | Complete trisomy 18 syndrome, E3 Trisomy, trisomy 18 |
| Mesh Id | D000073842 |
| Mesh Label | Trisomy 18 Syndrome |
| Mesh Subclassof | D000015, D006330, D025063 |
| Doid Label | Edwards syndrome |
| Doid Description | A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18. OMIM mapping confirmed by DO. [LS]. |
| Disease Node Id | disease_node_262 |
| Doid Id | DOID_1085 |
| Label | Trisomy 18 Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Duplication Syndrome(ID:disease_node_13621) (Disease)