 | Naam onderzoek | Code | |
|---|
 Autoimmuunziekten | |
| Biologics | |
| Bloedcelchemie rood | |
| Bloedcelchemie wit | |
| Bloedstolling | |
| Bloedstolling CITO | |
| Cryobiologie | |
| Erytrocytenserologie | |
| Erytrocytenserologie pre-nataal | |
| HLA-onderzoek | |
| Immunochemie | |
| Immunocytologie | |
| OLVG Lab B.V. Klinische Chemie | |
| OLVG Lab B.V. Medische Microbiologie | |
 Trombo-/Leukocyten serologie | |
| ADP receptor defect gen panel | X027 | |
| Amegakaryocytaire trombocytopenie met radio-ulnaire synostose gen panel | X028 | |
| Autosomaal dominante trombocytopenie 2 gen panel | X030 | |
| Autosomaal dominante trombocytopenie 4 gen panel | X031 | |
| Bernard-Soulier syndroom gen panel | X032 | |
| Chediak-Higashi syndroom gen panel | X034 | |
| Congenitale amegakaryocytaire trombocyopenie (CAMT) gen panel | X035 | |
| Dense granulae afwijkingen gen panel | X038 | |
| Familiaire plaatjes disorder met predispositie voor AML gen panel | X041 | |
| Ghosal hematodiaphyseal dysplasia syndrome gen panel | X042 | |
| Granulocyten, auto-antistoffen tegen | T913 | |
| Granulocytopenie van de pasgeborene | T914 | |
| Gray platelet like syndroom gen panel | X045 | |
| Gray platelet syndroom gen panel | X044 | |
| Hemorrhagische diathese door glycoproteine VI deficientie gen panel | X033 | |
| Heparin induced platelet activation assay (HIPAA) | T041 | |
| Heparine geïnduceerde trombocytopenie (HIT) | T040 | |
| Hermansky-Pudlak syndroom gen panel | X046 | |
| HPA-1a en/of HPA-5b genotypering in maternaal plasma, foetaal | T012 | |
| HPA antistoffen tegen trombocyten en genotypering bij refractairiteit na trombocytentransfusie | T928 | |
| Immuuntrombocytopenie (ITP) | T924 | |
| Laag Frequente Humane Plaatjes Antigenen onderzoek gen panel | X067 | |
| Leukocyte integrin adhesion deficientie, type III gen panel | X047 | |
| Macrotrombocytopenie en sensorineurale doofheid | X049 | |
| Macrotrombocytopenie, β-tubuline 1 gerelateerd gen panel | X048 | |
| May-Hegglin en andere MYH9 afwijkingen gen panel | X050 | |
| Pari-Trousseau trombocytopenie en Jacobson syndroom gen panel | X052 | |
| Plaatjes-type bloeding aandoening 18 gen panel | X054 | |
| Plaatjes-type von Willebrand ziekte gen panel | X053 | |
| Prenatale verdenking foetale alloimmuun trombocytopenie | T923 | |
| Quebec platelet disorder gen panel | X055 | |
| Refractairiteit na trombocytentransfusie | T902 | |
| Scott syndroom gen panel | X056 | |
| Transfusion Related Acute Lung Injury (TRALI ) | T903 | |
| Trombocytenantigenen, HPA-1, (-2), -3, -5 en of 15 genotypering | T021 | |
| Trombocytopathie, onduidelijke onderliggende pathologie gen panel | X062 | |
| Trombocytopenie absent radius (TAR) syndroom gen panel | X059 | |
| Trombocytopenie door geneesmiddelen (goud therapie) | T907 | |
| Trombocytopenie en gevoeligheid voor kanker gen panel | X058 | |
| Trombocytopenie en trombocytemie 1 (THCYT1) gen panel | X036 | |
| Trombocytopenie na transfusie (PTP) | T906 | |
| Trombocytopenie van de pasgeborene (of foetus) | T911 | |
| Trombocytopenie van de pasgeborene, vervolgonderzoek: 2 a 3 weken na de partus | T919 | |
| Trombocytopenie van de pasgeborene, vervolgonderzoek: 20e week, volgende zwangerschap | T920 | |
| Trombopoietine | T023 | |
| Tromboxane A2 receptor defect gen panel | X063 | |
| Wiskott-Aldrich syndroom (X-linked trombocytopenie) gen panel | X060 | |
| X-linked trombocytopenie met dyserytropoiesis gen panel | X061 | |
| Ziekte van Glanzmann gen panel | X043 | |
| Virusdiagnostiek | |
| (Not Categorized) | |
