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dystonie 28 (aandoening)
dystonie 28
DYT28
Dystonia 28
DYT28 - dystonia 28
Lysine methyltransferase 2B-related dystonia
KMT2B-related dystonia
A rare persistent combined dystonia characterized by childhood onset of progressive dystonia typically beginning in the lower limbs and eventually progressing to generalized dystonia with involvement of the upper limbs, trunk, face and neck. Variable developmental delay and intellectual disability, along with mild microcephaly, short stature, abnormal eye movements and slightly dysmorphic facial features have been reported in association.
Id1281844004
StatusPrimitive
Clinical courseprogressief
InterpretsMovement
SNOMED CT to Orphanet simple map589618
SNOMED CT to ICD-10 extended map
TargetG24.8
RuleTRUE
AdviceALWAYS G24.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified