Gamstorp-Wohlfart Syndrome
Disease ID: disease_node_20383
Connections displayed (default: 10).
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| Dbxref | GARD:12353, MIM:137200 |
|---|---|
| Subclassof | DOID_225 |
| Data Source | DOID |
| Synonyms | autosomal recessive neuromyotonia and axonal neuropathy, myokymia, myotonia and muscle wasting |
| Doid Label | Gamstorp-Wohlfart syndrome |
| Doid Description | A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs. OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000363 |
| Disease Node Id | disease_node_20383 |
| Doid Id | DOID_0050526 |
| Label | Gamstorp-Wohlfart Syndrome |
- Outgoing r'ship
HAS_SYMPTOMto/from Progressive Weakness(ID:disease_node_21078) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)