Acrocephalosyndactyly type V
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Pfeiffer syndrome type 2 (disorder)
Pfeiffer syndrome type 2
acrocefalosyndactylie type 5 subtype 2
syndroom van Pfeiffer type 2
Pfeiffer-syndroom type 2
Id1003916008
StatusPrimitive
Associated morphologyCongenital abnormal fusion
Finding siteDigit structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyCongenital premature fusion
Finding siteJoint structure of suture of skull
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified