geneMAP
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Basic Information
- Primary DI
- D-TRMF000028405SMN1MRT5J5
- Basic UDI-DI Code
- B-TRMF000028405SMN1MRT5J5
- Reference
- SMN1M-RT50
- Device Types
- None provided
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
Additional Description
Spinal Muscular Atrophy (SMA), progressive degeneration of the spinal cord and brainstem nuclei and anterior It is a disease characterized by muscle weakness and atrophy resulting from the loss of horn cells. SMA is an autosomal recessive disorder caused by mutations in the SMN1 (Survival Motor Neuron) gene. is a disease. Approximately 94% of SMA patients can be detected by commonly used molecular assays. SMN1 lacks both copies of exons 7 and 8, while carrier individuals have one copy
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0106010199 | MONOGENETIC DISORDERS TESTS - OTHER |
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).