splenic disease
- Coding system
- SNOMED CT
- Organisation
- PRIMIS Covid Vaccination Uptake Reporting
- Codelist ID
- primis-covid19-vacc-uptake/spln_cov_cod
- Version Tag
- v.1.5.3
- Version ID
- 04704ad3
Versions
- v.1.5.3
Description
Taken from the SPLN_COV_COD fields in SARS-CoV2 (COVID-19) Vaccine Uptake Reporting Codes v.1.5.3
References
| code | term |
|---|---|
| 1003551006 | Agenesis of spleen |
| 10759351000119103 | Sickle cell anemia in mother complicating childbirth |
| 111572002 | beta^0^ Thalassemia, nondeletion type |
| 123617004 | Fleckmilz |
| 1239371000000103 | Haemoglobin E beta zero thalassaemia |
| 1239381000000101 | Haemoglobin E beta plus thalassaemia |
| 127040003 | Sickle cell-hemoglobin SS disease |
| 127041004 | Sickle cell-beta-thalassemia |
| 127042006 | Sickle cell beta plus thalassemia |
| 127047000 | Sickle cell-hemoglobin Lepore disease |
| 127048005 | Sickle cell-Hemoglobin O Arab disease |
| 161626009 | History of splenectomy |
| 1671000 | Sago spleen |
| 174776001 | Total splenectomy |
| 174778000 | Total splenectomy and reimplantation of fragments |
| 174789007 | Embolization of spleen |
| 17604001 | Bilateral right-sidedness sequence |
| 195340002 | Embolism and thrombosis of the splenic artery |
| 197478000 | Congenital celiac disease |
| 197479008 | Acquired celiac disease |
| 205735005 | Hypoplasia of spleen |
| 210193004 | Spleen massive parenchymal disruption with open wound into cavity |
| 22996003 | Splenic infarction |
| 23269001 | Double heterozygous sickling disorder |
| 234319005 | Splenectomy |
| 234391009 | Sickle cell anemia with high hemoglobin F |
| 234392002 | Hemoglobin E/beta thalassemia disease |
| 234510005 | Amyloidosis of spleen |
| 236854007 | Septic splenitis |
| 23761004 | Hyposplenism |
| 25472008 | Sickle cell-hemoglobin D disease |
| 262821002 | Avulsion of spleen |
| 26682008 | Homozygous beta thalassemia |
| 27080008 | beta^0^ Thalassemia, deletion type |
| 275403002 | Villous atrophy |
| 275404008 | Celiac rickets |
| 275405009 | Partial villous atrophy |
| 300564004 | Spleen absent |
| 302961007 | Hereditary splenic hypoplasia |
| 314118002 | Laparoscopic total splenectomy |
| 33479006 | Distal subtotal pancreatectomy with splenectomy and pancreaticojejunostomy |
| 35434009 | Sickle cell-hemoglobin C disease |
| 38096003 | Functional asplenia |
| 38970002 | Doan-Wright syndrome |
| 396330006 | Celiac crisis |
| 396331005 | Celiac disease |
| 416180004 | Hemoglobin SS disease without crisis |
| 416214006 | Sickle cell-hemoglobin D disease without crisis |
| 416290001 | Hemoglobin S sickling disorder without crisis |
| 416484003 | Sickle cell-hemoglobin E disease with crisis |
| 416638004 | Sickle cell-hemoglobin E disease without crisis |
| 416826005 | Sickle cell-thalassemia disease with crisis |
| 417048006 | Sickle cell-thalassemia disease without crisis |
| 417279003 | Hemoglobin S sickling disorder with crisis |
| 417357006 | Sickling disorder due to hemoglobin S |
| 417425009 | Hemoglobin SS disease with crisis |
| 417517009 | Sickle cell-hemoglobin C disease with crisis |
| 417683006 | Sickle cell-hemoglobin C disease without crisis |
| 417748003 | Sickle cell-hemoglobin D disease with crisis |
| 440206000 | Hemoglobin SS disease with vasoocclusive crisis |
| 444108000 | Acute sickle cell splenic sequestration crisis |
| 45259000 | Celiac infantilism |
| 47024008 | Sickle cell-hemoglobin E disease |
| 54006005 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia |
| 56338005 | Splenic fibrosis |
| 58381000 | Hypersplenism |
| 60194009 | Distal subtotal pancreatectomy with splenectomy |
| 61535006 | Transplantation of spleen |
| 61715008 | Celiac disease with diffuse intestinal ulceration |
| 700050004 | Overwhelming infection in asplenic patient |
| 700051000 | Sepsis in asplenic subject |
| 700052007 | Post-splenectomy sepsis |
| 702624008 | Aplasia of spleen |
| 707147002 | Asplenia |
| 711407000 | Thrombocytopathy, asplenia and miosis |
| 717156002 | Biliary atresia with splenic malformation syndrome |
| 722386009 | Celiac disease with epilepsy and cerebral calcification syndrome |
| 724639003 | Asplenia following surgical procedure |
| 726708009 | Familial isolated congenital asplenia |
| 73190000 | epsilon gamma delta beta^0^ Thalassemia |
| 75451007 | Thalassemia major |
| 76336008 | Delta beta zero thalassemia |
| 770593004 | Refractory celiac disease |
| 783254003 | Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome |
| 82893001 | Splenic atrophy |
| 861371000000102 | Acquired absence of spleen |
| 86715000 | Beta zero thalassemia |
| 89810003 | ^A^gamma delta beta^0^ thalassemia |
| 91867008 | Adult form of celiac disease |
| 93030006 | Congenital absence of spleen |
| 93292008 | Congenital hypoplasia of spleen |
| 95846001 | Red blood cell sequestration in spleen |
Codes not in the full codelist are in faint grey.