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syndroom van malformatie van onderste extremiteit en hypospadie (aandoening)
syndroom van malformatie van onderste extremiteit en hypospadie
syndroom van Fried-Goldberg-Mundel
syndroom van misvorming van been en hypospadie
Fried-Goldberg-Mundel-syndroom
Lower limb malformation hypospadias syndrome
Fried Goldberg Mundel syndrome
A rare developmental defect during embryogenesis with characteristics of severe, unilateral or bilateral lower limb malformations (including tibial hypoplasia, split and rocker bottom-shaped feet, and oligo syndactyly), normal upper limbs and hypospadias. Additional dysmorphic features (for example short neck and low-set, large ears), atrial septal defect, ureteropelvic junction stenosis and slight septation of the spleen, have also been reported. There have been no further descriptions in the literature since 1977.
Id770561007
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ74.2
TermOverige congenitale misvormingen van onderste extremiteit(en), inclusief bekkengordel
TargetQ54.9
TermHypospadie, niet gespecificeerd
SNOMED CT to Orphanet simple map2487
SNOMED CT to ICD-10 extended map
TargetQ87.2
RuleTRUE
AdviceALWAYS Q87.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified