6011000124106~MAPADVICE~IF ENAMEL-RENAL SYNDROME CHOOSE K00.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~E83.52
447562003~MAPRULE~TRUE
447562003~MAPRULE~IFA 700112007 | Bartter syndrome type 4 (disorder) |
6011000124106~MAPTARGET~E83.59
447562003~MAPTARGET~E26.8
6011000124106~MAPPRIORITY~7
6011000124106~MAPPRIORITY~4
447562003~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 1 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPRULE~IFA 725033008 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days
6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE E83.42 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPADVICE~ALWAYS N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE
6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
447562003~MAPGROUP~2
447562003~MAPRULE~IFA 236445002 | Macroscopic nephrocalcinosis (disorder) |
6011000124106~MAPRULE~IFA 59531002 | Tryptophan malabsorption syndrome |
447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
447562003~MAPADVICE~IF MICROSCOPIC NEPHROCALCINOSIS CHOOSE N29.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPRULE~IFA 276584001 | Neonatal nephrocalcinosis (disorder) |
447562003~MAPPRIORITY~5
447562003~MAPGROUP~1
6011000124106~MAPTARGET~P70.4
447562003~CORRELATIONID~447561005
6011000124106~MAPADVICE~ALWAYS E83.59
447562003~MAPRULE~OTHERWISE TRUE
6011000124106~MAPADVICE~IF ENAMEL-RENAL SYNDROME CHOOSE N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447637006
447562003~MAPRULE~IFA 700107006 | Bartter syndrome antenatal type 1 (disorder) |
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF OXALOSIS CHOOSE E72.53 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P71.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPTARGET~E70.8
6011000124106~MAPRULE~IFA 1269271003 | Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome |
447562003~MAPRULE~IFA 700109009 | Bartter syndrome antenatal type 2 (disorder) |
447562003~MAPRULE~IFA 59531002 | Tryptophan malabsorption syndrome (disorder) |
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~
900000000000497000~MAPTARGET~C3547
447562003~MAPPRIORITY~1
447562003~MAPADVICE~IF BARTTER SYNDROME TYPE 4 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447637006
447562003~MAPTARGET~N29.8
6011000124106~MAPRULE~IFA 109477002 | Enamel-renal syndrome |
447562003~MAPRULE~IFA 236444003 | Microscopic nephrocalcinosis (disorder) |
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPADVICE~ALWAYS E83.59 | DESCENDANTS NOT EXHAUSTIVELY MAPPED
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF ATYPICAL FANCONI SYNDROME, NEONATAL HYPERINSULINISM SYNDROME CHOOSE E72.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 725033008 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement |
447562003~MAPADVICE~IF NEONATAL NEPHROCALCINOSIS CHOOSE P96.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~3
6011000124106~MAPADVICE~IF ATYPICAL FANCONI SYNDROME, NEONATAL HYPERINSULINISM SYNDROME CHOOSE P70.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPTARGET~P96.8
6011000124106~MAPADVICE~IF TRYPTOPHAN MALABSORPTION SYNDROME CHOOSE E72.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447639009
6011000124106~MAPPRIORITY~1
447562003~MAPADVICE~IF BARTTER SYNDROME ANTENATAL TYPE 2 CHOOSE E26.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~6
6011000124106~CORRELATIONID~447561005
447562003~MAPADVICE~IF TRYPTOPHAN MALABSORPTION SYNDROME CHOOSE E70.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF FAMILIAL PRIMARY HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS WITHOUT SEVERE OCULAR INVOLVEMENT CHOOSE E83.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~E83.42
447562003~MAPPRIORITY~2
6011000124106~MAPRULE~TRUE
6011000124106~MAPTARGET~E72.53
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
6011000124106~MAPTARGET~N29
6011000124106~MAPRULE~IFA 373607009 | Oxalosis |
6011000124106~MAPPRIORITY~2
6011000124106~MAPTARGET~E72.09
447562003~MAPADVICE~IF MACROSCOPIC NEPHROCALCINOSIS CHOOSE N29.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPTARGET~E83.5
6011000124106~MAPADVICE~ALWAYS N29 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | DESCENDANTS NOT EXHAUSTIVELY MAPPED
6011000124106~MAPTARGET~K00.5
6011000124106~MAPTARGET~P71.2
447562003~MAPCATEGORYID~447638001
447562003~MAPADVICE~ALWAYS E83.5
447562003~MAPPRIORITY~4
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