autosomaal dominante hereditaire aandoening
congenitale afwijking van ulna
congenitale dysplasie van extremiteit
hereditaire aandoening van bewegingsapparaat
hereditaire ontwikkelingsstoornis
metafysaire chondrodysplasie
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syndroom van dysplasie van ulnaire metafysen (aandoening)
syndroom van dysplasie van ulnaire metafysen
syndroom van Rosenberg-Lohr
Ulna metaphyseal dysplasia syndrome
Rosenberg-Lohr syndrome
Id715242008
StatusPrimitive
Associated morphologydysplasie
Finding sitebotstructuur van ulna
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Has interpretationonder referentiebereik
InterpretsBody height
SNOMED CT to Orphanet simple map
SNOMED CT to ICD-10 extended map
TargetQ78.5
RuleTRUE
AdviceALWAYS Q78.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified