6011000124106~MAPADVICE~IF ALPORT SYNDROME, INTELLECTUAL DISABILITY, MIDFACE HYPOPLASIA, ELLIPTOCYTOSIS SYNDROME CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~D58.1
6011000124106~MAPRULE~IFA 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 (disorder) |
447562003~MAPRULE~TRUE
6011000124106~MAPRULE~IFA 75443009 | Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) |
6011000124106~MAPRULE~IFA 234410008 | Hereditary elliptocytosis with transient poikilocytosis (disorder) |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO BETA SPECTRIN DEFECT IN SELF-ASSOCIATION CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 720982007 | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) |
6011000124106~MAPRULE~IFA 66262001 | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction |
6011000124106~MAPTARGET~F78.A9
6011000124106~MAPPRIORITY~7
6011000124106~MAPPRIORITY~4
6011000124106~MAPRULE~IFA 73073009 | Hereditary elliptocytosis due to beta spectrin defect in self-association |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS WITH TRANSIENT POIKILOCYTOSIS CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPADVICE~ALWAYS D58.1
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPRULE~IFA 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 |
447562003~MAPADVICE~ALWAYS D58.1
6011000124106~MAPPRIORITY~8
900000000000497000~MAPTARGET~D101.
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO ABNORMAL PROTEIN 4.1 CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPGROUP~1
6011000124106~MAPTARGET~F79
6011000124106~MAPRULE~IFA 8857001 | Hereditary elliptocytosis due to alpha spectrin defect |
447562003~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO DEFICIENCY OF PROTEIN 4.1 CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~R71.8
6011000124106~MAPRULE~IFA 15121005 | Hereditary elliptocytosis due to glycophorin C deficiency |
447562003~MAPTARGET~D58.1
6011000124106~MAPTARGET~Q87.81
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO ALPHA SPECTRIN DEFECT CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPGROUP~4
6011000124106~MAPRULE~IFA 8857001 | Hereditary elliptocytosis due to alpha spectrin defect (disorder) |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO BETA SPECTRIN-ANKYRIN INTERACTION CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~9
6011000124106~MAPRULE~IFA 73073009 | Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) |
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF ALPORT SYNDROME, INTELLECTUAL DISABILITY, MIDFACE HYPOPLASIA, ELLIPTOCYTOSIS SYNDROME CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF ALPORT SYNDROME, INTELLECTUAL DISABILITY, MIDFACE HYPOPLASIA, ELLIPTOCYTOSIS SYNDROME CHOOSE Q87.81 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF ALPORT SYNDROME, INTELLECTUAL DISABILITY, MIDFACE HYPOPLASIA, ELLIPTOCYTOSIS SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS WITH TRANSIENT POIKILOCYTOSIS CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO ABNORMAL PROTEIN 4.1 CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 66262001 | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder) |
6011000124106~MAPRULE~IFA 75443009 | Hereditary elliptocytosis due to abnormal protein 4.1 |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO BETA SPECTRIN DEFECT IN SELF-ASSOCIATION CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO GLYCOPHORIN C DEFICIENCY CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~6
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO BETA SPECTRIN-ANKYRIN INTERACTION CHOOSE R71.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF ALPORT SYNDROME, INTELLECTUAL DISABILITY, MIDFACE HYPOPLASIA, ELLIPTOCYTOSIS SYNDROME CHOOSE Q18.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 234410008 | Hereditary elliptocytosis with transient poikilocytosis |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO ALPHA SPECTRIN DEFECT CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~3
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO DEFICIENCY OF PROTEIN 4.1 CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~3
6011000124106~MAPRULE~IFA 15121005 | Hereditary elliptocytosis due to glycophorin C deficiency (disorder) |
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
6011000124106~MAPTARGET~Q18.8
6011000124106~MAPRULE~IFA 720982007 | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
6011000124106~MAPADVICE~IF HEREDITARY ELLIPTOCYTOSIS DUE TO GLYCOPHORIN C DEFICIENCY CHOOSE D58.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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