6011000124106~MAPTARGET~N04.9
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME DUE TO CONGENITAL INFECTION CHOOSE B99.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q15.9
447562003~MAPRULE~TRUE
6011000124106~MAPADVICE~IF FINNISH CONGENITAL NEPHROTIC SYNDROME CHOOSE N04.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000497000~MAPTARGET~K01w.
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME WITH FOCAL GLOMERULOSCLEROSIS CHOOSE N04.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 722118005 | Congenital nephrotic syndrome due to congenital infection |
6011000124106~MAPRULE~IFA 722369003 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis |
6011000124106~MAPRULE~IFA 236384008 | Congenital nephrotic syndrome with focal glomerulosclerosis |
6011000124106~MAPPRIORITY~4
6011000124106~MAPRULE~IFA 721297008 | Galloway Mowat syndrome |
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME, INTERSTITIAL LUNG DISEASE, EPIDERMOLYSIS BULLOSA SYNDROME CHOOSE Q81.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 236385009 | Drash syndrome (disorder) |
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPRULE~IFA 236384008 | Congenital nephrotic syndrome with focal glomerulosclerosis (disorder) |
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPRULE~IFA 236385009 | Drash syndrome |
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPRULE~IFA 197601003 | Finnish congenital nephrotic syndrome (disorder) |
6011000124106~MAPRULE~IFA 236383002 | Familial mesangial sclerosis (disorder) |
6011000124106~MAPADVICE~IF PIERSON SYNDROME CHOOSE Q15.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 723449004 | Pierson syndrome |
6011000124106~MAPRULE~IFA 721297008 | Galloway Mowat syndrome (disorder) |
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPTARGET~N26.9
447562003~MAPGROUP~1
6011000124106~MAPADVICE~IF DRASH SYNDROME CHOOSE N04.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF GALLOWAY MOWAT SYNDROME CHOOSE Q40.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 733453005 | Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome |
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPADVICE~ALWAYS N04.9 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
6011000124106~MAPADVICE~IF GALLOWAY MOWAT SYNDROME CHOOSE N04.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~N04.8
6011000124106~MAPTARGET~J84.9
6011000124106~MAPADVICE~IF FAMILIAL MESANGIAL SCLEROSIS CHOOSE N26.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME DUE TO DIFFUSE MESANGIAL SCLEROSIS CHOOSE N04.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~N04.3
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPRULE~IFA 733453005 | Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 18.0 years
6011000124106~MAPPRIORITY~5
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPRULE~IFA 722118005 | Congenital nephrotic syndrome due to congenital infection (disorder) |
6011000124106~MAPRULE~IFA 197601003 | Finnish congenital nephrotic syndrome |
6011000124106~MAPTARGET~Q81.9
6011000124106~MAPPRIORITY~1
6011000124106~MAPTARGET~N04.1
6011000124106~MAPRULE~IFA 236383002 | Familial mesangial sclerosis |
6011000124106~MAPPRIORITY~6
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME, INTERSTITIAL LUNG DISEASE, EPIDERMOLYSIS BULLOSA SYNDROME AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 18.0 YEARS CHOOSE J84.848 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~ALWAYS N04.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE
6011000124106~MAPADVICE~IF GALLOWAY MOWAT SYNDROME CHOOSE Q02 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q02
6011000124106~MAPTARGET~B99.9
6011000124106~MAPRULE~IFA 722369003 | Congenital nephrotic syndrome due to diffuse mesangial sclerosis (disorder) |
6011000124106~MAPADVICE~IF CONGENITAL NEPHROTIC SYNDROME, INTERSTITIAL LUNG DISEASE, EPIDERMOLYSIS BULLOSA SYNDROME CHOOSE J84.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
6011000124106~MAPTARGET~Q40.1
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
447562003~MAPTARGET~N04.9
6011000124106~MAPTARGET~J84.848
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