Oculopharyngodistal Myopathy
Disease ID: disease_node_18966
Connections displayed (default: 10).
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| Dbxref | GARD:12592, MIM:PS164310, ORDO:98897 |
|---|---|
| Subclassof | DOID_423 |
| Data Source | DOID |
| Doid Label | oculopharyngodistal myopathy |
| Doid Description | A myopathy that is characterized by progressive external ocular, facial and pharyngeal muscle weakness, leading to variable degrees of ptosis, ophthalmoparesis, facial muscle atrophy, dysarthria and dysphagia, as well as distal muscle weakness and atrophy of lower and upper extremities. |
| Disease Node Id | disease_node_18966 |
| Doid Id | DOID_0081296 |
| Label | Oculopharyngodistal Myopathy |
- Incoming r'ship
SUBCLASS_OFto/from Oculopharyngodistal Myopathy 1(ID:disease_node_18970) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Muscular Diseases(ID:disease_node_5316) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculopharyngodistal Myopathy 4(ID:disease_node_18967) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculopharyngodistal Myopathy 3(ID:disease_node_18968) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Oculopharyngodistal Myopathy 2(ID:disease_node_18969) (Disease)