Arthrogryposis Multiplex Congenita
Disease ID: disease_node_20565
Connections displayed (default: 10).
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| Dbxref | GARD:777, MIM:PS617468 |
|---|---|
| Subclassof | DOID_863, DOID_0080015, DOID_0050737 |
| Data Source | DOID |
| Doid Label | arthrogryposis multiplex congenita |
| Doid Description | A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20565 |
| Doid Id | DOID_0080954 |
| Disease Has Basis In | HP_0001197 |
| Label | Arthrogryposis Multiplex Congenita |
- Incoming r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita-1(ID:disease_node_20569) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita-5(ID:disease_node_20566) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita-4(ID:disease_node_20567) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita-6(ID:disease_node_20570) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Arthrogryposis Multiplex Congenita-3(ID:disease_node_20568) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Nervous System Diseases(ID:disease_node_5531) (Disease)