CCSD Schedule
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| Code | Description | Chapter | Guidance | Coding principles |
|---|---|---|---|---|
| 0515B | Fibrinogen (Clauss) level |
34.2.0 Haematology |
false | |
| 0515G | Myotubular myopathy (genetic) |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8186B |
false |
| 0516G | Neurofibromatosis 1 (NF1) |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8187B |
false |
| 0517G | PCDH19 |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8189B |
false |
| 0518G | Pelizaeus-Merzbacher disease |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8190B |
false |
| 0519G | PMP22 Gene |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8191B |
false |
| 0520B | Peripheral blood film |
34.2.0 Haematology |
false | |
| 0520G | PRSS1 / SPINK 1 |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8194B |
false |
| 0521G | RAPSN mutation |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8195B |
false |
| 0522G | Marfan syndrome FBN1 |
34.1.3 Biochemistry Genetic Analysis |
Replaces code 8174B |
false |