Marfan Syndrome
Disease ID: disease_node_5011
Connections displayed (default: 10).
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| Dbxref | GARD:6975, ICD10CM:Q87.4, ICD9CM:759.82, MESH:D008382, MIM:154700, NCI:C34807, SNOMEDCT_US_2023_03_01:19346006, UMLS_CUI:C0024796 |
|---|---|
| Subclassof | DOID_520, DOID_5614, DOID_65 |
| Data Source | DOID, MESH |
| Synonyms | Marfan's syndrome |
| Disease Has Location | UBERON_0000947, UBERON_0000970 |
| Mesh Id | D008382 |
| Mesh Label | Marfan Syndrome |
| Mesh Subclassof | D003240, D030342, D006330, D000015, D001848 |
| Doid Label | Marfan syndrome |
| Doid Description | A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_5011 |
| Doid Id | DOID_14323 |
| Label | Marfan Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Aortic Diseases(ID:disease_node_1295) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Connective Tissue Diseases(ID:disease_node_2242) (Disease)