diff --git a/.github/workflows/schema.yml b/.github/workflows/schema.yml index 2faa760..d50ee52 100644 --- a/.github/workflows/schema.yml +++ b/.github/workflows/schema.yml @@ -29,7 +29,7 @@ jobs: cd pyxb_build python setup.py bdist_wheel - - uses: actions/upload-artifact@v2 + - uses: actions/upload-artifact@v4 with: name: ukrdc_schema_wheel path: pyxb_build/dist/*.whl @@ -66,7 +66,7 @@ jobs: ./build.sh python setup.py bdist_wheel - - uses: actions/upload-artifact@v2 + - uses: actions/upload-artifact@v4 with: name: ukrdc_xsdata_wheel path: xsdata_build/dist/*.whl @@ -86,7 +86,7 @@ jobs: if: startsWith(github.ref, 'refs/tags/') steps: - - uses: actions/download-artifact@v2 + - uses: actions/download-artifact@v4 - name: Release uses: softprops/action-gh-release@v1 diff --git a/codes/code_lists/ukrr_observations.csv b/codes/code_lists/ukrr_observations.csv index 04ff0fa..9c6b5d0 100644 --- a/codes/code_lists/ukrr_observations.csv +++ b/codes/code_lists/ukrr_observations.csv @@ -1,61 +1,147 @@ UKRR,QBLA1,Serum Creatinine,result +UKRR,QBLA2,Date of serum creatinine,result UKRR,QBLA3,Serum Urea,result UKRR,QBLA4,Serum Bicarbonate,result +UKRR,QBLA5,Date of bicarbonate,result UKRR,QBLA6,Serum Sodium,result +UKRR,QBLA7,Date of sodium,result UKRR,QBLA9,Serum Potassium,result +UKRR,QBLAA,Date of potassium,result UKRR,QBLAB,Lab Calculated eGFR,result UKRR,QBLAC,Serum Uric Acid (Urate),result +UKRR,QBLAD,Date of serum uric acid (urate),result +UKRR,QBLAJ,Date of serum urea,result UKRR,QBLAL,Unit Calculated eGFR,result +UKRR,QBLAP,Glomerular filtration rate (GFR) predicted by creatinine based formula (CKD-EPI) WITHOUT ethnicity,result +UKRR,QBLAQ,Date of CKD-EPI eGFR,result +UKRR,QBLAR,Glomerular filtration rate (GFR) predicted by creatinine based formula (MDRD) WITHOUT ethnicity,result +UKRR,QBLAS,Date of MDRD eGFR,result UKRR,QBLB1,Serum Phosphate,result +UKRR,QBLB2,Date of serum phosphate,result UKRR,QBLB3,Serum Calcium,result +UKRR,QBLBB,Date of serum calcium,result UKRR,QBLB4,Corrected Serum Calcium,result +UKRR,QBLBC,Date of corrected/adjusted serum calcium,result UKRR,QBLB5,Serum Alkaline Phosphatase,result +UKRR,QBLB6,Date of Serum alkaline phosphatase,result UKRR,QBLB7,Serum Albumin,result +UKRR,QBLB8,Date of albumin,result UKRR,QBLB9,Serum Parathyroid Hormone (PTH),result +UKRR,QBLBA,Date of PTH,result UKRR,QBLC1,Urine Protein:Creatinine Ratio,result +UKRR,QBLC2,Date of urine protein:creatinine ratio2,result UKRR,QBLC3,Urine Albumin:Creatinine Ratio,result +UKRR,QBLC4,Date of urine albumin:creatinine ratio,result UKRR,QBLD1,Total Serium Cholesterol,result +UKRR,QBLD2,Date of serum cholesterol,result UKRR,QBLD3,Serum HDL Cholesterol,result +UKRR,QBLDB,Date of serum HDL cholesterol,result UKRR,QBLD4,Serum LDL Cholesterol,result +UKRR,QBLDC,Date of serum LDL cholesterol,result UKRR,QBLD5,Serum Triglycerides,result +UKRR,QBLDF,Date of serum triglycerides,result UKRR,QBLD6,CRP,result +UKRR,QBLD7,Date of CRP,result UKRR,QBLD8,Hba1c %,result UKRR,QBLDA,Hba1c,result +UKRR,QBLD9,Date of HbA1c,result UKRR,QBLE1,Haemoglobin,result UKRR,QBLE3,MCH,result UKRR,QBLE4,Platelets,result +UKRR,QBLE9,Date of platelets,result UKRR,QBLE5,WBC (from full blood count),result +UKRR,QBLEA,Date of WBC,result UKRR,QBLEB,Haemloglobin,result +UKRR,QBLE2,Date of haemoglobin,result UKRR,QBLF1,Serum Ferritin,result +UKRR,QBLF2,Date of serum ferritin,result UKRR,QBLF3,Transferrin Saturation,result +UKRR,QBLF4,Date of transferrin saturation,result UKRR,QBLF5,Percentage of Hypochromic Cells,result +UKRR,QBLF6,Date of hypochromic red cells,result UKRR,QBLF7,Serum B12,result +UKRR,QBLF8,Date of serum B12,result UKRR,QBLF9,Serum Folate,result +UKRR,QBLFA,Date of serum folate,result UKRR,QBLFB,Red Cell Folate,result +UKRR,QBLFC,Date of red cell folate,result UKRR,QBLFD,Serum Aluminium,result UKRR,QBLFF,Tacrolimus Blood Concentration Level,result +UKRR,QBLFG,Date of tacrolimus blood concentration level,result UKRR,QBLFH,Sirolimus Blood Concentration Level,result +UKRR,QBLFJ,Date of sirolimus blood concentration level,result UKRR,QBLFK,Ciclosporin Blood Concentration Level,result +UKRR,QBLFL,Date of ciclosporin blood concentration level,result UKRR,QBLFM,Mycophenolate Blood Concentration Level,result +UKRR,QBLFN,Date of mycophenolate blood concentration level,result UKRR,QBLG1,Weight,observation +UKRR,QBLG2,Date of weight,observation UKRR,QBLG3,Systolic BP,observation UKRR,QBLG4,Diastolic BP,observation +UKRR,QBLG5,Date of Blood Pressure,observation +UKRR,QBLG6,Post dialysis systolic blood pressure,observation +UKRR,QBLG7,Post dialysis diastolic blood pressure,observation +UKRR,QBLG8,Date of post dialysis blood pressure,observation UKRR,QBLG9,Urea Reduction Ratio,result +UKRR,QBLGA,Date of urea reduction ratio,result UKRR,QBLGG,Kt/V,result +UKRR,QBLGH,Date of Kt/V,result UKRR,QBLGB,Height,observation +UKRR,QBLGC,Date of Height,observation +UKRR,QBLKS,Body weight measured post dialysis,observation +UKRR,QBLKT,Date of body weight measured post dialysis,observation +UKRR,QBLKU,Symptoms of peritonitis,observation +UKRR,QBLKV,Date of peritonitis symptoms,observation +UKRR,QBLGN,COVID-19 antigen PCR,result +UKRR,QBLGP,Date of COVID-19 antigen PCR,result +UKRR,QBLGS,COVID-19 IgG antibody status,result +UKRR,QBLGT,Date of COVID-19 IgG antibody status,result +UKRR,QBLGU,PSA - prostate specific antigen,result +UKRR,QBLGV,Date of PSA test,result +UKRR,QBLH1,BK Virus status,result +UKRR,QBLH2,Date of BK Virus status,result UKRR,QBLHA,HBV Antibody Status,result +UKRR,QBLHB,Date of test HBV surface antibody,result UKRR,QBLHC,HBV Surface Antigen Status,result +UKRR,QBLHD,Date of test HBV surface antigen,result UKRR,QBLHE,HCV Antibody Status,result +UKRR,QBLHF,Date of test HCV surface antibody,result UKRR,QBLHG,CMV Antibody Status,result UKRR,QBLHK,CMV PCR Copies/ML,result UKRR,QBLHM,HIV Antigen Status,result +UKRR,QBLHL,Date HIV screening test,result UKRR,QBLHN,Varicella,result UKRR,QBLHR,EBV Status,result UKRR,QBLHS,EBV Log Count,result +UKRR,QBLHU,Date of urine volume in 24 hours,result UKRR,QBLHV,Urine Volume in 24 Hours,observation UKRR,QBLHX,Urinary Creatinine Extraction,result +UKRR,QBLHY,Date of urine creatinine concentration,result +UKRR,QBLKE,Serum creatinine - post dialysis,result +UKRR,QBLKF,Date of post dialysis creatinine,result +UKRR,QBLKG,Serum urea - post dialysis,result +UKRR,QBLKH,Date of post dialysis urea,result +UKRR,QBLKL,Serum potassium - post dialysis,result +UKRR,QBLKM,Date of post dialysis potassium,result +UKRR,QBLKN,Serum sodium - post dialysis,result +UKRR,QBLKP,Date of post dialysis sodium,result +UKRR,QBLKQ,Serum bicarbonate - post dialysis,result +UKRR,QBLKR,Date of post dialysis bicarbonate,result UKRR,QBLPA,PTH ULN,result UKRR,QBLPB,PTH / PTHH ULN Ratio,result UKRR,QBLPC,ALT,result +UKRR,QBLJB,Date of ALT,result +UKRR,QBLJJ,Reticulocyte haemoglobin (CHr),result +UKRR,QBLJK,Date of reticulocyte haemoglobin,result +UKRR,QBLJL,Proteinuria dipstick test,result +UKRR,QBLJM,Date of Proteinuria dipstick test,result +UKRR,QBLJN,PD fluid WCC count,result +UKRR,QBLJP,Date of PD fluid WCC count,result +UKRR,QBLJQ,PD fluid culture organism grown text,result +UKRR,QBLJR,Date of PD fluid culture test,result +UKRR,QBLJS,Urine protein concentration,result +UKRR,QBLJT,Date of urinary protein concentration,result +UKRR,QBLJX,Blood culture organism grown text **,result +UKRR,QBLJY,Date of blood culture test,result UKRR,QBLPD,ANC,result UKRR,QBLPE,ALC,result \ No newline at end of file diff --git a/schema/ukrdc/CHANGELOG.md b/schema/ukrdc/CHANGELOG.md index 0641f0c..19ea706 100644 --- a/schema/ukrdc/CHANGELOG.md +++ b/schema/ukrdc/CHANGELOG.md @@ -1,5 +1,15 @@ # Changelog +## 4.3.0 - ??? +### Changed +- Make Treatment/AdmitReason mandatory +- Make Treatment/HealthCareFacility mandatory +- Make Medication/FromTime mandatory +- Increase Max Length of SendingFacility +- Add "IND" to InterpretationCodes +- 111 (COVID 19) has been added to the EDTA_COD code list. +- Modify PRD and COD Types - remove the enumeration so any SNOMED code can be submitted + ## 4.2.0 - 2024-02-26 ### Changed - Restricted Treatment/VisitDescription to 255 characters @@ -35,7 +45,9 @@ - Amended Treatment to remove items not in V5. - Added V5 Treatment Modality Codes. - +## 3.5.0 - 2023-09-15 +### Changed +- Add 101 (First Seen) to the RR7 Treatment List ### 3.4.5 - 2023-06-14 ### Changed diff --git a/schema/ukrdc/Encounters/Treatment.xsd b/schema/ukrdc/Encounters/Treatment.xsd index 19a5c07..f6be2bb 100644 --- a/schema/ukrdc/Encounters/Treatment.xsd +++ b/schema/ukrdc/Encounters/Treatment.xsd @@ -39,13 +39,13 @@ Responsible Clinician as a National Clinicial code where possible or other local code if not. - + Treatment Centre (TXT20) - + Modality diff --git a/schema/ukrdc/LabOrders/LabOrder.xsd b/schema/ukrdc/LabOrders/LabOrder.xsd index 67fafcf..25dbab1 100644 --- a/schema/ukrdc/LabOrders/LabOrder.xsd +++ b/schema/ukrdc/LabOrders/LabOrder.xsd @@ -306,6 +306,11 @@ Unknown + + + Indeterminate + + diff --git a/schema/ukrdc/Medications/Medication.xsd b/schema/ukrdc/Medications/Medication.xsd index 4ace4a8..37c357c 100644 --- a/schema/ukrdc/Medications/Medication.xsd +++ b/schema/ukrdc/Medications/Medication.xsd @@ -5,6 +5,7 @@ + @@ -24,7 +25,7 @@ - + @@ -44,37 +45,11 @@ Where the Medicine was Prescribed - + Medication Route - - - - - - - - - - - - - - - - - - - - - - - - - - diff --git a/schema/ukrdc/Types/CF_EDTA_COD.xsd b/schema/ukrdc/Types/CF_EDTA_COD.xsd index 37c3e3b..6f06182 100644 --- a/schema/ukrdc/Types/CF_EDTA_COD.xsd +++ b/schema/ukrdc/Types/CF_EDTA_COD.xsd @@ -6,338 +6,22 @@ + + + + Code values for COD are maintained in the Registry Codes repository https://github.com/renalreg/registry-codes: + - tables/code_list/edta_cod.csv + + Any valid SNOMED CT code may be submitted when CodingStandard = SNOMED. + + - - - Cause of death uncertain / not determined - - - - - Myocardial Ischaemia and Infraction - - - - - Hyperkalaemia - - - - - Haemorrhagic Pericarditis - - - - - Other causes of cardiac failure - - - - - Cardiac arrest/sudden death; other cause or unknown - - - - - Hypertensive cardiac failure - - - - - Hypokalaemia - - - - - Fluid Overload / Pulmonary Oedema - - - - - Elevated PVR / Pulmonary hypertension - - - - - Pulmonary Embolus - - - - - Cerebro-Vascular Accident, other cause or unspecified - - - - - Gastro-Intestinal Haemorrhage (Digestive) - - - - - Haemorrhage from graft site - - - - - Haemorrhage from vascular access or dailysis circuit - - - - - Cerebral haemorrhage from ruptured vascular aneurysm (not code 22 or 23) - - - - - Haemorrhage from surgery (except digestive haemorrhage - - - - - Other haemorrhage, other site and/or other cause - - - - - Mesenteric Infarction - - - - - Pulmonary Infection (Bacterial) - - - - - Pulmonary Infection (Viral) - - - - - Pulmonary Infection (Fungal or Protozoal; parasitic) - - - - - Infections elsewhere (except viral hepatitis) - - - - - Septicaemia - - - - - Tuberculosis (Lung) - - - - - Tuberculosis (Elsewhere) - - - - - Generalised Viral Infection - - - - - Peritonitis (all causes except for Peritoneal Dialysis) - - - - - Liver disease due to hepatitis B virus - - - - - Liver disease due to other viral hepatitis - - - - - Liver disease due to drug toxicity - - - - - Cirrhosis - not viral (alcoholic or other cause) - - - - - Cystic liver disease - - - - - Liver failure - cause unknown - - - - - Patient refused further treatment for ERF - - - - - Suicide - - - - - ERF Treatment ceased for any other reason - - - - - ERF TReatment withdrawn for medical reasons - - - - - Uremia caused by graph failure - - - - - Pancreatitis - - - - - Bone Marrow Depression (Aplosia) - - - - - Cachexia - - - - - Malignant disease in patient treated by immuosuppressive therapy - - - - - Malignant disease: solid tumours except those of 66 - - - - - Malignant disease: lymphoproliferative disorders (Except 66) - - - - - Dementia - - - - - Peritonitis (sclerosing, with peritoneal dialysis) - - - - - Perforation of peptic ulcer - - - - - Perforation of colon - - - - - - COPD - - - - - Multi-system failure - - - - - Accident related to ERF Treatment - - - - - Accident unrelated to ERF Treatment - - - - - Cause of death uncertain/not determined - - - - - Peritonitis (bacterial, with peritoneal dialysis) - - - - - Peritonitis (fungal, with peritoneal dialysis) - - - - - Peritonitis (due to other cause, with peritoneal dialysis) - - - - - Peripheral Vascular Disease - - - - - Calciphylaxis - - - - - Ischaemic bowel - - - - - Ruptured AAA - - - - - Advanced CKD not on dialysis (conservative management) - - - - - Acute Kidney Injury - - - - - C Diff Colitis - - - - - Line Related Sepsis - - + diff --git a/schema/ukrdc/Types/CF_EDTA_PRD.xsd b/schema/ukrdc/Types/CF_EDTA_PRD.xsd index 5e504d6..8b86636 100644 --- a/schema/ukrdc/Types/CF_EDTA_PRD.xsd +++ b/schema/ukrdc/Types/CF_EDTA_PRD.xsd @@ -12,2934 +12,19 @@ + + + Code values for PRD are maintained in the Registry Codes repository https://github.com/renalreg/registry-codes: + - tables/code_list/edta_prd.csv + - tables/code_list/edta2.csv + - tables/code_list/snomed_renal_diagnosis.csv + + Any valid SNOMED CT code may be submitted when CodingStandard = SNOMED. + + - - - Chronic Renal Failure, Aetiology uncertain - - - - - Glomerulonephritis, historically not examined - - - - - Severe nephoritic syndrome with focal sclerosis (Paediatric) - - - - - IgA nephropathy proven by immunofluoresence - - - - - Dense deposite disease, membrano-prolif. GN Type II - - - - - Membranous nephropathy - - - - - Membrano-proliferative GN Type I - - - - - Rapidly progressive GN without systemic disease (crescentic) - - - - - Focal segmental glomeruloscerosis with nephrotic syndrome in adults - - - - - Glomerulonephritis, historically examined - - - - - Pyelo/Interstital nephritis - cause not specified - - - - - Pyelo/Interstital nephritis - with neurogenic bladder - - - - - Pyelo/Interstital nephritis - congen. obst. uropathy +/- reflux - - - - - Pyelo/Interstital nephritis - acquired obst. uropathy - - - - - Pyelo/Interstital nephritis - vesico-ureteric reflux no obstruction - - - - - Pyelo/Interstital nephritis - due to urolithiasis - - - - - Pyelo/Interstital nephritis - due to other cause (please specify) - - - - - Tubulo interstital nephritis (not pyelonephritis) - - - - - Nephropathy due to analgesic drugs - - - - - Nephropathy due to cis-platinum - - - - - Nephropathy due to Cyclosporin A - - - - - Lead induced nephropathy (interstitial) - - - - - Nephroapthy caused by other specific drug - - - - - Cystic Kidney Disease - Type Unspecified - - - - - Polycystic Kidneys - Adult Type (Dominant) - - - - - Polycystic Kidneys = Infantile (Recessive) - - - - - Medullary Cystic Disease - including Nephoronophthisis - - - - - Cystic Kidney Disease - Other Specified Type - - - - - Hereditary/Familial Nephropathy - Typoe Unspecified - - - - - Hereditary Nephritis with Nerve Deafness (Alport's) - - - - - Cystinosis - - - - - Primary Oxalosis - - - - - Fabry's disease - - - - - Hereditary Nephropathy - Other - - - - - congenital Renal Hypoplasia - Type Unspecified - - - - - Oligomeganephronic Hypoplasia - - - - - Congenital Renal Dysplasia +/- Urinary Tract Malformation - - - - - Syndrome of Agenesis of Abdo. muscles - Prune Belly Syndrome - - - - - Renal Vascular Disease - Type Unspecified - - - - - Renal Vascular Disease due to MALIGNANT Hypertension - - - - - Renal Vascular Disease due to Hypertension - - - - - Renal Vascular Disease due to Polyarteritis - - - - - Wegener's Granulomatosis - - - - - Ischaemic Renal Disease/Cholesterol Embolism - - - - - Glomerulonephritis related to liver cirrhosis - - - - - Cryoglobulinaemic Glomerulonephritis - - - - - Renal Vascular Disease - Classified (Please Specify) - - - - - Diabetes Type 1 (Insulin Dependent) - - - - - Diabetes Type 2 (Non-Insulin Dependent) - - - - - Myelomatosis - - - - - Amyloid - - - - - Systemic Lupus Erythematosus - - - - - Henoch-Schonlein Purpura - - - - - Goodpastures Syndrome - - - - - Scleroderma - - - - - Haemolytic Uraemic Syndrome - - - - - Multu-System Diseased - Type Unspecified - - - - - Cortical or Tubula Necrosis - - - - - Tuberculosis - - - - - Gout - - - - - Nephrocalcinosis / Hypercalcaemic Nephropathy - - - - - Balkan Nephropathy - - - - - Kidney Tumour - - - - - Traumatic or Surgical Loss of Kidney - - - - - Other identified Renal Disorders - Please Specify - - - - - - Adult Nephrotic Syndrome - No Histology - - - - - Nephrotic Syndrome Of Childhood - Steroid Sensitive - No Histology - - - - - Congenital Nephrotic Syndrome (Cns) - No Histology - - - - - Congenital Nephrotic Syndrome (Cns) - Finnish Type - No Histology - - - - - Congenital Nephrotic Syndrome (Cns) - Finnish Type - Histologically Proven - - - - - Congenital Nephrotic Syndrome (Cns) - Diffuse Mesangial Sclerosis - - - - - Congenital Nephrotic Syndrome (Cns) - Focal Segmental Glomerulosclerosis (Fsgs) - - - - - Denys-Drash Syndrome - - - - - Congenital Nephrotic Syndrome (Cns) - Congenital Infection - - - - - Minimal Change Nephropathy - No Histology - - - - - Minimal Change Nephropathy - Histologically Proven - - - - - Iga Nephropathy - No Histology - - - - - Iga Nephropathy - Histologically Proven - - - - - Familial Iga Nephropathy - No Histology - - - - - Familial Iga Nephropathy - Histologically Proven - - - - - Iga Nephropathy Secondary To Liver Cirrhosis - No Histology - - - - - Iga Nephropathy Secondary To Liver Cirrhosis - Histologically Proven - - - - - Igm - Associated Nephropathy - - - - - Membranous Nephropathy - Idiopathic - - - - - Membranous Nephropathy - Malignancy Associated - - - - - Membranous Nephropathy - Drug Induced - - - - - Membranous Nephropathy - Infection Associated - - - - - Mesangiocapillary Glomerulonephritis Type 1 - - - - - Mesangiocapillary Glomerulonephritis Type 2 (Dense Deposit Disease) - - - - - Mesangiocapillary Glomerulonephritis Type 3 - - - - - Idiopathic Rapidly Progressive (Crescentic) Glomerulonephritis - - - - - Primary Focal Segmental Glomerulosclerosis (Fsgs) - - - - - Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - No Histology - - - - - Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Recessive - Histologically Proven - - - - - Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - No Histology - - - - - Familial Focal Segmental Glomerulosclerosis (Fsgs) - Autosomal Dominant - Histologically Proven - - - - - Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - No Histology - - - - - Focal Segmental Glomerulosclerosis (Fsgs) Secondary To Obesity - Histologically Proven - - - - - Diffuse Endocapillary Glomerulonephritis - - - - - Mesangial Proliferative Glomerulonephritis - - - - - Focal And Segmental Proliferative Glomerulonephritis - - - - - Glomerulonephritis - Secondary To Other Systemic Disease - - - - - Glomerulonephritis - Histologically Indeterminate - - - - - Systemic Vasculitis - Anca Negative - Histologically Proven - - - - - Systemic Vasculitis - Anca Positive - No Histology - - - - - Granulomatosis With Polyangiitis - No Histology - - - - - Granulomatosis With Polyangiitis - Histologically Proven - - - - - Microscopic Polyangiitis - Histologically Proven - - - - - Churg-Strauss Syndrome - No Histology - - - - - Churg-Strauss Syndrome - Histologically Proven - - - - - Polyarteritis Nodosa - - - - - Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - No Histology - - - - - Anti-Glomerular Basement Membrane (Gbm) Disease / Goodpasture'S Syndrome - Histologically Proven - - - - - Systemic Lupus Erythematosus / Nephritis - No Histology - - - - - Systemic Lupus Erythematosus / Nephritis - Histologically Proven - - - - - Henoch-Schonlein Purpura / Nephritis - No Histology - - - - - Henoch-Schonlein Purpura / Nephritis - Histologically Proven - - - - - Renal Scleroderma / Systemic Sclerosis - No Histology - - - - - Renal Scleroderma / Systemic Sclerosis - Histologically Proven - - - - - Essential Mixed Cryoglobulinaemia - No Histology - - - - - Essential Mixed Cryoglobulinaemia - Histologically Proven - - - - - Cryoglobulinaemia Secondary To Hepatitis C - No Histology - - - - - Cryoglobulinaemia Secondary To Hepatitis C - Histologically Proven - - - - - Cryoglobulinaemia Secondary To Systemic Disease - No Histology - - - - - Cryoglobulinaemia Secondary To Systemic Disease - Histologically Proven - - - - - Primary Reflux Nephropathy - Sporadic - - - - - Familial Reflux Nephropathy - - - - - Congenital Dysplasia / Hypoplasia - - - - - Multicystic Dysplastic Kidneys - - - - - Dysplasia Due To Fetal Ace-Inhibitor Exposure - - - - - Glomerulocystic Disease - - - - - Congenital Pelvi-Ureteric Junction Obstruction - - - - - Congenital Vesico-Ureteric Junction Obstruction - - - - - Posterior Urethral Valves - - - - - Syndrome Of Agenesis Of Abdominal Muscles - Prune Belly Syndrome - - - - - Congenital Neurogenic Bladder - - - - - Bladder Exstrophy - - - - - Megacystis-Megaureter - - - - - Oligomeganephronia - - - - - Renal Papillary Necrosis - Cause Unknown - - - - - Acquired Obstructive Uropathy / Nephropathy - - - - - Acquired Obstructive Nephropathy Due To Neurogenic Bladder - - - - - Obstructive Nephropathy Due To Prostatic Hypertrophy - - - - - Obstructive Nephropathy Due To Prostate Cancer - - - - - Obstructive Nephropathy Due To Bladder Cancer - - - - - Obstructive Nephropathy Due To Other Malignancies - - - - - Idiopathic Retroperitoneal Fibrosis - - - - - Retroperitoneal Fibrosis Secondary To Malignancies - - - - - Calculus Nephropathy / Urolithiasis - - - - - Calcium Oxalate Urolithiasis - - - - - Enteric Hyperoxaluria - - - - - Magnesium Ammonium Phosphate (Struvite) Urolithiasis - - - - - Uric Acid Urolithiasis - - - - - Tubulointerstitial Nephritis - No Histology - - - - - Tubulointerstitial Nephritis - Histologically Proven - - - - - Familial Interstitial Nephropathy - No Histology - - - - - Familial Interstitial Nephropathy - Histologically Proven - - - - - Tubulointerstitial Nephritis Associated With Autoimmune Disease - No Histology - - - - - Tubulointerstitial Nephritis Associated With Autoimmune Disease - Histologically Proven - - - - - Tubulointerstitial Nephritis With Uveitis (Tinu) - No Histology - - - - - Tubulointerstitial Nephritis With Uveitis (Tinu) - Histologically Proven - - - - - Renal Sarcoidosis - No Histology - - - - - Renal Sarcoidosis - Histologically Proven - - - - - Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - No Histology - - - - - Aristolochic Acid Nephropathy (Balkan / Chinese Herb / Endemic Nephropathy) - Histologically Proven - - - - - Drug-Induced Tubulointerstitial Nephritis - No Histology - - - - - Drug-Induced Tubulointerstitial Nephritis - Histologically Proven - - - - - Nephropathy Due To Analgesic Drugs - No Histology - - - - - Nephropathy Due To Analgesic Drugs - Histologically Proven - - - - - Nephropathy Due To Ciclosporin - No Histology - - - - - Nephropathy Due To Ciclosporin - Histologically Proven - - - - - Nephropathy Due To Tacrolimus - No Histology - - - - - Nephropathy Due To Tacrolimus - Histologically Proven - - - - - Nephropathy Due To Aminoglycosides - No Histology - - - - - Nephropathy Due To Aminoglycosides - Histologically Proven - - - - - Nephropathy Due To Amphotericin - No Histology - - - - - Nephropathy Due To Amphotericin - Histologically Proven - - - - - Nephropathy Due To Cisplatin - No Histology - - - - - Nephropathy Due To Cisplatin - Histologically Proven - - - - - Nephropathy Due To Lithium - No Histology - - - - - Nephropathy Due To Lithium - Histologically Proven - - - - - Lead Induced Nephropathy - No Histology - - - - - Lead Induced Nephropathy - Histologically Proven - - - - - Acute Urate Nephropathy - No Histology - - - - - Acute Urate Nephropathy - Histologically Proven - - - - - Chronic Urate Nephropathy - Histologically Proven - - - - - Radiation Nephritis - - - - - Renal / Perinephric Abscess - - - - - Renal Tuberculosis - - - - - Leptospirosis - - - - - Hantavirus Nephropathy - - - - - Xanthogranulomatous Pyelonephritis - - - - - Nephropathy Related To Hiv - No Histology - - - - - Nephropathy Related To Hiv - Histologically Proven - - - - - Schistosomiasis - - - - - Other Specific Infection - - - - - Diabetic Nephropathy In Type I Diabetes - No Histology - - - - - Diabetic Nephropathy In Type I Diabetes - Histologically Proven - - - - - Diabetic Nephropathy In Type Ii Diabetes - No Histology - - - - - Diabetic Nephropathy In Type Ii Diabetes - Histologically Proven - - - - - Chronic Hypertensive Nephropathy - No Histology - - - - - Chronic Hypertensive Nephropathy - Histologically Proven - - - - - Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - No Histology - - - - - Malignant Hypertensive Nephropathy / Accelerated Hypertensive Nephropathy - Histologically Proven - - - - - Ageing Kidney - No Histology - - - - - Ischaemic Nephropathy - No Histology - - - - - Ischaemic Nephropathy / Microvascular Disease - Histologically Proven - - - - - Renal Artery Stenosis - - - - - Atheroembolic Renal Disease - No Histology - - - - - Atheroembolic Renal Disease - Histologically Proven - - - - - Fibromuscular Dysplasia Of Renal Artery - - - - - Renal Arterial Thrombosis / Occlusion - - - - - Renal Vein Thrombosis - - - - - Cardiorenal Syndrome - - - - - Hepatorenal Syndrome - - - - - Renal Amyloidosis - - - - - Aa Amyloid Secondary To Chronic Inflammation - - - - - Al Amyloid Secondary To Plasma Cell Dyscrasia - - - - - Familial Amyloid Secondary To Protein Mutations - No Histology - - - - - Familial Amyloid Secondary To Protein Mutations - Histologically Proven - - - - - Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - No Histology - - - - - Familial Aa Amyloid Secondary To Familial Mediterranean Fever / Traps (Hibernian Fever) - Histologically Proven - - - - - Myeloma Kidney - No Histology - - - - - Myeloma Cast Nephropathy - Histologically Proven - - - - - Light Chain Deposition Disease - - - - - Immunotactoid / Fibrillary Nephropathy - - - - - Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Associated - - - - - Atypical Haemolytic Uraemic Syndrome (Hus) - Diarrhoea Negative - - - - - Thrombotic Thrombocytopenic Purpura (Ttp) - - - - - Haemolytic Uraemic Syndrome (Hus) Secondary To Systemic Disease - - - - - Congenital Haemolytic Uraemic Syndrome (Hus) - - - - - Familial Haemolytic Uraemic Syndrome (Hus) - - - - - Familial Thrombotic Thrombocytopenic Purpura (Ttp) - - - - - Nephropathy Due To Pre-Eclampsia / Eclampsia - - - - - Sickle Cell Nephropathy - No Histology - - - - - Sickle Cell Nephropathy - Histologically Proven - - - - - Autosomal Dominant (Ad) Polycystic Kidney Disease - - - - - Autosomal Dominant (Ad) Polycystic Kidney Disease Type I - - - - - Autosomal Dominant (Ad) Polycystic Kidney Disease Type Ii - - - - - Autosomal Recessive (Ar) Polycystic Kidney Disease - - - - - Alport Syndrome - No Histology - - - - - Alport Syndrome - Histologically Proven - - - - - Benign Familial Haematuria - - - - - Thin Basement Membrane Disease - - - - - Cystic Kidney Disease - - - - - Medullary Cystic Kidney Disease Type I - - - - - Medullary Cystic Kidney Disease Type Ii - - - - - Uromodulin-Associated Nephropathy (Familial Juvenile Hyperuricaemic Nephropathy) - - - - - Nephronophthisis - - - - - Nephronophthisis - Type 1 (Juvenile Type) - - - - - Nephronophthisis - Type 2 (Infantile Type) - - - - - Nephronophthisis - Type 3 (Adolescent Type) - - - - - Nephronophthisis - Type 4 (Juvenile Type) - - - - - Nephronophthisis - Type 5 - - - - - Nephronophthisis - Type 6 - - - - - Primary Fanconi Syndrome - - - - - Tubular Disorder As Part Of Inherited Metabolic Diseases - - - - - Dent Disease - - - - - Lowe Syndrome (Oculocerebrorenal Syndrome) - - - - - Inherited Aminoaciduria - - - - - Cystinuria - - - - - Cystinosis - - - - - Inherited Renal Glycosuria - - - - - Hypophosphataemic Rickets X-Linked (Xl) - - - - - Hypophosphataemic Rickets Autosomal Recessive (Ar) - - - - - Primary Renal Tubular Acidosis (Rta) - - - - - Proximal Renal Tubular Acidosis (Rta) - Type Ii - - - - - Distal Renal Tubular Acidosis (Rta) - Type I - - - - - Distal Renal Tubular Acidosis With Sensorineural Deafness - Gene Mutations - - - - - Nephrogenic Diabetes Insipidus - - - - - Lesch Nyhan Syndrome - Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency - - - - - Phosphoribosyl Pyrophosphate Synthetase (Prpps) Superactivity - - - - - Alagille Syndrome - - - - - Bartter Syndrome - - - - - Gitelman Syndrome - - - - - Liddle Syndrome - - - - - Apparent Mineralocorticoid Excess - - - - - Glucocorticoid Suppressible Hyperaldosteronism - - - - - Inherited / Genetic Diabetes Mellitus Type Ii - - - - - Pseudohypoaldosteronism Type 1 - - - - - Pseudohypoaldosteronism Type 2 (Gordon Syndrome) - - - - - Familial Hypocalciuric Hypercalcaemia - - - - - Familial Hypercalciuric Hypocalcaemia - - - - - Familial Hypomagnesaemia - - - - - Primary Hyperoxaluria - - - - - Primary Hyperoxaluria Type I - - - - - Primary Hyperoxaluria Type Ii - - - - - Fabry Disease - No Histology - - - - - Fabry Disease - Histologically Proven - - - - - Xanthinuria - - - - - Nail-Patella Syndrome - - - - - Rubinstein-Taybi Syndrome - - - - - Tuberous Sclerosis - - - - - Von Hippel-Lindau Disease - - - - - Medullary Sponge Kidneys - - - - - Horse-Shoe Kidney - - - - - Frasier Syndrome - - - - - Branchio-Oto-Renal Syndrome - - - - - Williams Syndrome - - - - - Townes-Brocks Syndrome - - - - - Lawrence-Moon-Biedl / Bardet-Biedl Syndrome - - - - - Mitochondrial Cytopathy - - - - - Familial Nephropathy - - - - - Acute Kidney Injury - - - - - Acute Kidney Injury Due To Hypovolaemia - - - - - Acute Kidney Injury Due To Circulatory Failure - - - - - Acute Kidney Injury Due To Sepsis - - - - - Acute Kidney Injury Due To Rhabdomyolysis - - - - - Acute Kidney Injury Due To Nephrotoxicity - - - - - Acute Cortical Necrosis - - - - - Acute Pyelonephritis - - - - - Kidney Tumour - - - - - Renal Cell Carcinoma - Histologically Proven - - - - - Transitional Cell Carcinoma - Histologically Proven - - - - - Wilms Tumour - Histologically Proven - - - - - Mesoblastic Nephroma - Histologically Proven - - - - - Single Kidney Identified In Adulthood - - - - - Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Caused By Tumour Nephrectomy - - - - - Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Traumatic Loss Of Kidney - - - - - Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) Due To Donor Nephrectomy - - - - - Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - No Histology - - - - - Chronic Kidney Disease (Ckd) / Chronic Renal Failure (Crf) - Aetiology Uncertain / Unknown - Histologically Proven - - - - - Haematuria And Proteinuria - No Histology - - - - - Nephrotic Syndrome Of Childhood - Steroid Resistant - No Histology - - - - - Nephrotic Syndrome Of Childhood - No Trial Of Steroids - No Histology - - - - - Renal Cysts And Diabetes Syndrome - - - - - Chronic Urate Nephropathy - No Histology - - - - - Chronic Renal Failure Due To Systemic Infection - - - - - Renal Coloboma Syndrome - - - - - Hypercalcaemic Nephropathy - - - - - Retroperitoneal Fibrosis Secondary To Peri-Aortitis - - - - - Retroperitoneal Fibrosis Secondary To Drugs - - - - - Renal Failure - - - - - Chronic Renal Failure - - - - - Isolated Haematuria - No Histology - - - - - Isolated Proteinuria - No Histology - - - - - Primary Hyperoxaluria Type Iii - - - - - Glomerulonephritis - No Histology - - - - - Focal segmental glomerulosclerosis (FSGS) secondary to HIV - - - - - Focal segmental glomerulosclerosis (FSGS) secondary to lithium - - - - - Focal segmental glomerulosclerosis (FSGS) secondary to sickle cell - - - - - Renal papillary necrosis caused by diabetes - - - - - Renal papillary necrosis caused by analgesics - - - - - Renal papillary necrosis caused by sickle cell - - - - - Kidney stones due to ARPT deficiency - - - - - Infiltration by lymphoma - histologically proven - - - - - Nephropathy due to pre-eclampsia - - - - - Systemic vasculitis - ANCA negative - no histology - - - - - Systemic vasculitis - ANCA positive - histologically proven - - - - - Glomerulonephritis (disorder) - - - - - Nephrotic syndrome (disorder) - - - - - Steroid sensitive nephrotic syndrome of childhood (disorder) - - - - - Steroid resistant nephrotic syndrome of childhood (disorder) - - - - - Childhood nephrotic syndrome (disorder) - - - - - Congenital nephrotic syndrome (disorder) - - - - - Finnish congenital nephrotic syndrome (disorder) - - - - - Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) - - - - - Congenital nephrotic syndrome with focal glomerulosclerosis (disorder) - - - - - Drash syndrome (disorder) - - - - - Congenital nephrotic syndrome due to congenital infection (disorder) - - - - - Minimal change disease (disorder) - - - - - Immunoglobulin A nephropathy (disorder) - - - - - Familial immunoglobulin A nephropathy (disorder) - - - - - Immunoglobulin A nephropathy associated with liver disease (disorder) - - - - - Immunoglobulin M nephropathy (disorder) - - - - - Idiopathic membranous glomerulonephritis (disorder) - - - - - Membranous glomerulonephritis due to malignant neoplastic disease (disorder) - - - - - Membranous glomerulonephritis caused by drug (disorder) - - - - - Membranous glomerulonephritis co-occurrent with infectious disease (disorder) - - - - - Mesangiocapillary glomerulonephritis, type I (disorder) - - - - - Mesangiocapillary glomerulonephritis, type II (disorder) - - - - - Mesangiocapillary glomerulonephritis type III (disorder) - - - - - Crescentic glomerulonephritis (disorder) - - - - - Focal segmental glomerulosclerosis (disorder) - - - - - Autosomal recessive focal segmental glomerulosclerosis (disorder) - - - - - Autosomal recessive focal segmental glomerulosclerosis (disorder) - - - - - Autosomal dominant focal segmental glomerulosclerosis (disorder) - - - - - Autosomal dominant focal segmental glomerulosclerosis (disorder) - - - - - Focal segmental glomerulosclerosis (disorder) - - - - - FSGS co-occurrent with human immunodefiency virus infection (disorder) - - - - - Focal segmental glomerulosclerosis caused by lithium (disorder) - - - - - Focal segmental glomerulosclerosis due to sickle cell disease (disorder) - - - - - Diffuse endocapillary proliferative glomerulonephritis (disorder) - - - - - Mesangial proliferative glomerulonephritis (disorder) - - - - - Focal AND segmental proliferative glomerulonephritis (disorder) - - - - - Glomerulonephritis (disorder) - - - - - Systemic vasculitis (disorder) - - - - - Wegener's granulomatosis (disorder) - - - - - Microscopic polyarteritis nodosa (disorder) - - - - - Allergic granulomatosis angiitis (disorder) - - - - - Polyarteritis nodosa (disorder) - - - - - Goodpasture's disease (disorder) - - - - - Goodpasture's syndrome (disorder) - - - - - Systemic lupus erythematosus glomerulonephritis syndrome (disorder) - - - - - Systemic lupus erythematosus glomerulonephritis syndrome (disorder) - - - - - Henoch-Schönlein purpura (disorder) - - - - - Renal involvement in scleroderma (disorder) - - - - - Essential mixed cryoglobulinemia (disorder) - - - - - Essential mixed cryoglobulinemia (disorder) - - - - - Cryoglobulinemia due to chronic hepatitis C (disorder) - - - - - Secondary cryoglobulinemia (disorder) - - - - - Non-obstructive reflux-associated chronic pyelonephritis (disorder) - - - - - Familial non-obstructive reflux-associated chronic pyelonephritis (disorder) - - - - - Renal dysplasia (disorder) - - - - - Multicystic renal dysplasia (disorder) - - - - - Renal dysplasia due to fetal exposure to angiotensin converting enzyme inhibitor (disorder) - - - - - Maturity-onset diabetes of the young, type 5 (disorder) - - - - - Familial hypoplastic, glomerulocystic kidney (disorder) - - - - - Congenital pelviureteric junction obstruction (disorder) - - - - - Congenital ureterovesical obstruction (disorder) - - - - - Congenital posterior urethral valves (disorder) - - - - - Prune belly syndrome (disorder) - - - - - Congenital neurogenic urinary bladder (finding) - - - - - Exstrophy of bladder sequence (disorder) - - - - - Megacystis-megaureter syndrome (disorder) - - - - - Oligomeganephronic hypoplasia of kidney (disorder) - - - - - Papillary necrosis (disorder) - - - - - Renal papillary necrosis due to diabetes mellitus (disorder) - - - - - Renal papillary necrosis caused by analgesic drug (disorder) - - - - - Renal papillary necrosis due to sickle cell disease (disorder) - - - - - Nephropathy due to acquired urinary tract obstruction (disorder) - - - - - Obstructive nephropathy due to neurogenic bladder (disorder) - - - - - Obstructive nephropathy due to benign prostatic hyperplasia (disorder) - - - - - Obstructive nephropathy due to carcinoma of prostate (disorder) - - - - - Obstructive nephropathy due to bladder cancer (disorder) - - - - - Obstructive nephropathy due to malignancy (disorder) - - - - - Idiopathic retroperitoneal fibrosis (disorder) - - - - - Malignant retroperitoneal fibrosis (disorder) - - - - - Drug-induced retroperitoneal fibrosis (disorder) - - - - - Retroperitoneal fibrosis (disorder) - - - - - Urolithiasis (disorder) - - - - - Calcium oxalate urolithiasis (disorder) - - - - - Enteric hyperoxaluria (disorder) - - - - - Magnesium ammonium phosphate urolithiasis (disorder) - - - - - Uric acid urolithiasis (disorder) - - - - - Interstitial nephritis (disorder) - - - - - Tubulointerstitial nephritis (disorder) - - - - - Granulomatous sarcoid nephropathy (disorder) - - - - - Toxic nephropathy (disorder) - - - - - Drug-induced interstitial nephritis (disorder) - - - - - Analgesic nephropathy (disorder) - - - - - Nephropathy induced by ciclosporin (disorder) - - - - - Nephropathy induced by tacrolimus (disorder) - - - - - Nephropathy induced by aminoglycoside (disorder) - - - - - Nephropathy induced by amphotericin (disorder) - - - - - Cis-platinum nephropathy (disorder) - - - - - Lithium nephropathy (disorder) - - - - - Nephropathy induced by lead (disorder) - - - - - Acute urate nephropathy (disorder) - - - - - Chronic urate nephropathy (disorder) - - - - - Hypercalcemic nephropathy (disorder) - - - - - Radiation nephritis (disorder) - - - - - Renal abscess (disorder) - - - - - Perirenal abscess (disorder) - - - - - Tuberculosis of kidney (disorder) - - - - - Leptospirosis (disorder) - - - - - Hemorrhagic nephroso-nephritis (disorder) - - - - - Xanthogranulomatous pyelonephritis (disorder) - - - - - Disorder of kidney co-occurrent with human immunodeficiency virus infection (disorder) - - - - - Urinary schistosomiasis (disorder) - - - - - Infectious disease (disorder) - - - - - Renal disorder associated with type I diabetes mellitus (disorder) - - - - - Renal disorder due to type 2 diabetes mellitus (disorder) - - - - - Hypertensive renal disease (disorder) - - - - - Malignant hypertensive renal disease (disorder) - - - - - Malignant hypertensive renal disease (disorder) - - - - - Age related reduction of renal function (finding) - - - - - Nephropathy due to ischemia (disorder) - - - - - Renal artery stenosis (disorder) - - - - - Atheroembolism of renal arteries (disorder) - - - - - Atheroembolism of renal arteries (disorder) - - - - - Hyperplasia of renal artery (disorder) - - - - - Renal artery occlusion (disorder) - - - - - Thrombosis of renal vein (disorder) - - - - - Cardiorenal syndrome (disorder) - - - - - Hepatorenal syndrome (disorder) - - - - - Amyloid nephropathy (disorder) - - - - - AA amyloidosis (disorder) - - - - - AL amyloidosis (disorder) - - - - - Familial visceral amyloidosis, Ostertag type (disorder) - - - - - Amyloid of familial Mediterranean fever (disorder) - - - - - Myeloma kidney (disorder) - - - - - Light chain deposition disease (disorder) - - - - - Fibrillary glomerulonephritis (disorder) - - - - - Diarrhea-associated hemolytic uremic syndrome (disorder) - - - - - Diarrhea-negative hemolytic uremic syndrome (disorder) - - - - - Thrombotic thrombocytopenic purpura (disorder) - - - - - Hemolytic uremic syndrome (disorder) - - - - - Congenital hemolytic uremic syndrome (disorder) - - - - - Familial hemolytic uremic syndrome (disorder) - - - - - Upshaw-Schulman syndrome (disorder) - - - - - Nephropathy following eclampsia (disorder) - - - - - Nephropathy following pre-eclampsia (disorder) - - - - - Sickle cell nephropathy (disorder) - - - - - Polycystic kidney disease, adult type (disorder) - - - - - Adult type polycystic kidney disease type 1 (disorder) - - - - - Adult type polycystic kidney disease type 2 (disorder) - - - - - Polycystic kidney disease, infantile type (disorder) - - - - - Hereditary nephritis (disorder) - - - - - Benign familial hematuria (disorder) - - - - - Thin basement membrane disease (disorder) - - - - - Cystic disease of kidney (disorder) - - - - - Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) - - - - - Autosomal dominant medullary cystic kidney disease with hyperuricemia (disorder) - - - - - Familial juvenile gout (disorder) - - - - - Nephronophthisis (disorder) - - - - - Juvenile nephronophthisis (disorder) - - - - - Infantile nephronophthisis (disorder) - - - - - Adolescent nephronophthisis (disorder) - - - - - Nephronophthisis type 4 (disorder) - - - - - Nephronophthisis type 5 (disorder) - - - - - Nephronophthisis type 6 (disorder) - - - - - Congenital Fanconi syndrome (disorder) - - - - - Renal tubulo-interstitial disorders in metabolic diseases (disorder) - - - - - Dent's disease (disorder) - - - - - Lowe syndrome (disorder) - - - - - Inherited aminoaciduria (disorder) - - - - - Cystinuria (disorder) - - - - - Cystinosis (disorder) - - - - - Familial renal glucosuria (disorder) - - - - - Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder) - - - - - Autosomal recessive hypophosphatemic vitamin D refractory rickets (disorder) - - - - - Renal tubular acidosis (disorder) - - - - - Proximal renal tubular acidosis (disorder) - - - - - Distal renal tubular acidosis (disorder) - - - - - Distal renal tubular acidosis co-occurrent with sensorineural deafness (disorder) - - - - - Nephrogenic diabetes insipidus (disorder) - - - - - Lesch-Nyhan syndrome (disorder) - - - - - Ribose-phosphate pyrophosphokinase overactivity (disorder) - - - - - Deficiency of adenine phosphoribosyl transferase (disorder) - - - - - Arteriohepatic dysplasia (disorder) - - - - - Bartter syndrome (disorder) - - - - - Gitelman syndrome (disorder) - - - - - Pseudoprimary hyperaldosteronism (disorder) - - - - - Syndrome of apparent mineralocorticoid excess (disorder) - - - - - Glucocorticoid-suppressible hyperaldosteronism (disorder) - - - - - Maturity onset diabetes of the young, type 2 (disorder) - - - - - Pseudohypoaldosteronism, type 1 (disorder) - - - - - Pseudohypoaldosteronism, type 2 (disorder) - - - - - Familial hypocalciuric hypercalcemia (disorder) - - - - - Autosomal dominant hypocalcemia (disorder) - - - - - Primary hypomagnesemia (disorder) - - - - - Primary hyperoxaluria (disorder) - - - - - Primary hyperoxaluria, type I (disorder) - - - - - Primary hyperoxaluria, type II (disorder) - - - - - Primary hyperoxaluria, type III (disorder) - - - - - Fabry's disease (disorder) - - - - - Xanthinuria (disorder) - - - - - Nail patella-like renal disease (disorder) - - - - - Rubinstein-Taybi syndrome (disorder) - - - - - Tuberous sclerosis syndrome (disorder) - - - - - Von Hippel-Lindau syndrome (disorder) - - - - - Medullary sponge kidney (disorder) - - - - - Horseshoe kidney (disorder) - - - - - Frasier syndrome (disorder) - - - - - Renal coloboma syndrome (disorder) - - - - - Melnick-Fraser syndrome (disorder) - - - - - Williams syndrome (disorder) - - - - - Townes syndrome (disorder) - - - - - Laurence-Moon syndrome (disorder) - - - - - Mitochondrial cytopathy (disorder) - - - - - Progressive hereditary glomerulonephritis without deafness (disorder) - - - - - Acute renal failure syndrome (disorder) - - - - - Acute kidney injury due to hypovolemia (disorder) - - - - - Acute kidney injury due to circulatory failure (disorder) - - - - - Acute kidney injury due to sepsis (disorder) - - - - - Crush syndrome (disorder) - - - - - Nephrotoxic acute renal failure (disorder) - - - - - Acute necrosis of cortex of kidney (disorder) - - - - - Acute pyelonephritis (disorder) - - - - - Neoplasm of kidney (disorder) - - - - - Clear cell carcinoma of kidney (disorder) - - - - - Transitional cell carcinoma of kidney (disorder) - - - - - Nephroblastoma (disorder) - - - - - Mesoblastic nephroma (disorder) - - - - - Lymphomatous infiltrate of kidney - - - - - Absent kidney (finding) - - - - - Chronic kidney disease following excision of renal neoplasm (disorder) - - - - - Chronic kidney disease due to traumatic loss of kidney (disorder) - - - - - Chronic kidney disease following donor nephrectomy (disorder) - - - - - Chronic renal failure syndrome (disorder) - - - - - Hematuria syndrome (disorder) - - - - - Proteinuria (finding) - - - - - Chronic kidney disease due to systemic infection (disorder) - - - - - Renal failure syndrome (disorder) - - + @@ -2952,4 +37,4 @@ - \ No newline at end of file + diff --git a/schema/ukrdc/Types/Location.xsd b/schema/ukrdc/Types/Location.xsd index e29f8ab..590ea14 100644 --- a/schema/ukrdc/Types/Location.xsd +++ b/schema/ukrdc/Types/Location.xsd @@ -14,7 +14,7 @@ - + diff --git a/schema/ukrdc/Types/Route.xsd b/schema/ukrdc/Types/Route.xsd new file mode 100644 index 0000000..debce35 --- /dev/null +++ b/schema/ukrdc/Types/Route.xsd @@ -0,0 +1,28 @@ + + + + + + + + + + + + + + + + + + + + + + + + + + + + \ No newline at end of file diff --git a/schema/ukrdc/Types/SendingFacility.xsd b/schema/ukrdc/Types/SendingFacility.xsd index c04bb1c..c7fc1d3 100644 --- a/schema/ukrdc/Types/SendingFacility.xsd +++ b/schema/ukrdc/Types/SendingFacility.xsd @@ -4,7 +4,7 @@ - +