Congenital Myopathy 4A
Disease ID: disease_node_18958
Connections displayed (default: 10).
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| Dbxref | MIM:255310 |
|---|---|
| Subclassof | DOID_0050736, DOID_0080015, DOID_0081337 |
| Data Source | DOID |
| Synonyms | CFTD, congenital fiber-type disproportion |
| Doid Label | congenital myopathy 4A |
| Doid Description | A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18958 |
| Doid Id | DOID_0080102 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Myopathy 4A |
- Incoming r'ship
SUBCLASS_OFto/from X-Linked Congenital Myopathy With Fiber-Type Disproportion(ID:disease_node_18959) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Congenital Myopathy(ID:disease_node_18926) (Disease)