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syndroom van gespleten hand, obstructie van urinewegen, spina bifida en diafragmadefect (aandoening)
syndroom van gespleten hand, obstructie van urinewegen, spina bifida en diafragmadefect
syndroom van gespleten hand, obstructieve uropathie, spina bifida en diafragmadefect
syndroom van Czeizel-Losonci
Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome
Czeizel Losonci syndrome
Split hand, urinary anomalies, spina bifida syndrome
An exceedingly rare severe congenital genetic malformation disorder with characteristics of split hand/split foot, hydronephrosis, and spina bifida. Spinal and skeletal manifestations were thoracolumbar scoliosis, spina bifida (spina bifida occulta or spina bifida cystic), Bochdalek diaphragmatic hernia and radial defects. There have been no further descriptions in the literature since 1987.
Id732927000
StatusPrimitive
Associated morphologyfusiedefect
Finding sitestructuur van hand
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyfusiedefect
Finding sitestructuur van arcus vertebrae
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified