Multiple Synostoses Syndrome
Disease ID: disease_node_15741
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:PS186500, ORDO:3237 |
|---|---|
| Subclassof | DOID_0050736, DOID_1934 |
| Data Source | DOID |
| Doid Label | multiple synostoses syndrome |
| Doid Description | A dysostosis that is characterized by characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15741 |
| Doid Id | DOID_0050794 |
| Label | Multiple Synostoses Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Dysostoses(ID:disease_node_2668) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Multiple Synostoses Syndrome 1(ID:disease_node_15745) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Multiple Synostoses Syndrome 3(ID:disease_node_15743) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Multiple Synostoses Syndrome 2(ID:disease_node_15744) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Multiple Synostoses Syndrome 4(ID:disease_node_15742) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)