Neurofibromatoses
Disease ID: disease_node_9133
Connections displayed (default: 10).
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| Dbxref | GARD:10420, ICD10CM:Q85.0, ICD9CM:237.7, MESH:D017253, NCI:C6727, ORDO:634518, SNOMEDCT_US_2023_03_01:19133005, UMLS_CUI:C0162678, UMLS_CUI:C0495632 |
|---|---|
| Subclassof | DOID_0050736, DOID_0080690 |
| Data Source | DOID, MESH |
| Mesh Id | D017253 |
| Mesh Label | Neurofibromatoses |
| Mesh Subclassof | D020752, D009386, D020271, D009455 |
| Doid Label | neurofibromatosis |
| Doid Description | This disease may be obsoleted in the future. Diseases previously classified as neurofibromatosis 2 (DOID:0111252) and neurofibromatosis 3 (DOID:0070480 and DOID:0070481) have been reclassified by international consensus as subclasses of schwannomatosis. For details refer to definition sources for neurofibromatosis 1 (DOID:0111253). |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_9133 |
| Doid Id | DOID_8712 |
| Label | Neurofibromatoses |
| Doid Alternate Ids | DOID_14750, DOID_8711, DOID_9137 |
- Incoming r'ship
SUBCLASS_OFto/from Neurofibromatosis 1(ID:disease_node_5553) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Rasopathy(ID:disease_node_19055) (Disease)