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syndroom van ectrodactylie van voet en centrale polydactylie (aandoening)
syndroom van ectrodactylie van voet en centrale polydactylie
SFMMP-syndroom
syndroom van gespleten voet en mesoaxiale polydactylie
Split-foot malformation, mesoaxial polydactyly syndrome
SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome
Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome
A rare genetic syndrome with limb malformations as a major feature with characteristics of unilateral or bilateral split-foot malformation, nail abnormalities of the hand and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described.
Id1172635005
StatusPrimitive
Has interpretationgestoord
Interpretsgehoorfunctie
Associated morphologyfusiedefect
Finding sitestructuur van voet
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
ICD-10 complex map reference set
TargetQ72.7
RuleTRUE
AdviceALWAYS Q72.7 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ70.0
RuleTRUE
AdviceALWAYS Q70.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ70.2
RuleTRUE
AdviceALWAYS Q70.2
CorrelationSNOMED CT source code to target map code correlation not specified