| hereditaire continue spiervezelactiviteit (aandoening) | | hereditaire continue spiervezelactiviteit | | erfelijke continue spiervezelactiviteit
| | Hereditary continuous muscle fiber activity | | A rare non-dystrophic myopathy characterized by generalized myokymia and increased muscle tone associated with delayed motor milestones, leg stiffness, spastic gait, hyperreflexia and Babinski sign. Symptoms may be worsened by febrile illness or anesthesia. |
| | Id | 1231178006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 972 |
| SNOMED CT to ICD-10 extended map | | Target | G71.1 | | Rule | TRUE | | Advice | ALWAYS G71.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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