Smith-Lemli-Opitz Syndrome
Disease ID: disease_node_9876
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| Dbxref | GARD:5683, ICD10CM:E78.72, MESH:D019082, MIM:270400, NCI:C85071, SNOMEDCT_US_2023_03_01:43929004, UMLS_CUI:C0175694 |
|---|---|
| Subclassof | DOID_3146 |
| Data Source | DOID, MESH |
| Synonyms | Rutledge lethal multiple congenital anomaly syndrome, Smith-Opitz-Inborn syndrome |
| Mesh Id | D019082 |
| Mesh Label | Smith-Lemli-Opitz Syndrome |
| Mesh Subclassof | D008052, D000015, D050171, D043202 |
| Doid Label | Smith-Lemli-Opitz syndrome |
| Doid Description | OMIM mapping confirmed by DO. [LS]. |
| Disease Node Id | disease_node_9876 |
| Doid Id | DOID_14692 |
| Label | Smith-Lemli-Opitz Syndrome |
| Doid Alternate Ids | DOID_4366 |
- Outgoing r'ship
SUBCLASS_OFto/from Lipid Metabolism, Inborn Errors(ID:disease_node_4772) (Disease)