6011000124106~MAPTARGET~Q93.2
6011000124106~MAPTARGET~Q82.9
447562003~MAPRULE~TRUE
6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE R64 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE R63.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~4
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~Q87.0
6011000124106~MAPTARGET~
6011000124106~MAPTARGET~P05.9
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPADVICE~IF MCCUNE ALBRIGHT SYNDROME CHOOSE Q78.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE Q82.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF LEGIUS SYNDROME CHOOSE Q85.01 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPTARGET~Q85.01
6011000124106~MAPTARGET~R63.0
447562003~MAPTARGET~L81.3
447562003~MAPGROUP~1
447562003~MAPRULE~IFA 703541007 | Neurofibromatosis type 1-like syndrome (disorder) |
6011000124106~MAPTARGET~Q82.8
6011000124106~MAPADVICE~IF CAFÉ-AU-LAIT SPOTS AND RING CHROMOSOME 11 CHOOSE Q93.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~CORRELATIONID~447561005
6011000124106~MAPRULE~IFA 1177178005 | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome |
447562003~MAPRULE~OTHERWISE TRUE
6011000124106~MAPRULE~IFA 726029005 | McCune Albright syndrome |
900000000000497000~MAPTARGET~M291.
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPRULE~IFA 403758009 | Café-au-lait spots and ring chromosome 11 |
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
447562003~MAPADVICE~IF NEUROFIBROMATOSIS TYPE 1-LIKE SYNDROME CHOOSE Q85.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~R64
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPGROUP~4
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~ALWAYS L81.3
6011000124106~MAPTARGET~Q78.1
6011000124106~MAPRULE~IFA 1300197001 | Mosaic Legius syndrome |
6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE L81.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE P05.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~MAPPRIORITY~6
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~IFA 782949007 | Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome |
6011000124106~MAPTARGET~L81.3
447562003~MAPPRIORITY~2
6011000124106~MAPRULE~IFA 703541007 | Legius syndrome |
6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE Q99.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~3
6011000124106~MAPADVICE~IF MOSAIC LEGIUS SYNDROME CHOOSE Q82.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPADVICE~ALWAYS L81.3
6011000124106~MAPADVICE~IF NEUROFIBROMATOSIS TYPE 1-LIKE SYNDROME CHOOSE Q85.01 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~3
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
447562003~MAPTARGET~Q85.8
6011000124106~MAPRULE~IFA 703541007 | Neurofibromatosis type 1-like syndrome (disorder) |
6011000124106~MAPTARGET~Q99.8
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