dwerggroei
hereditaire ontwikkelingsstoornis
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groeiachterstand door resistentie tegen insulineachtige groeifactor 1 (aandoening)
groeiachterstand door resistentie tegen insulineachtige groeifactor 1
groeivertraging door resistentie tegen somatomedine C
groeivertraging door IGF-1-resistentie
Growth delay due to insulin-like growth factor I resistance
Growth delay due to insulin-like growth factor 1 resistance
Somatomedin C resistance
IGF-1 (insulin-like growth factor 1) resistance
Growth delay due to IGF-I resistance is characterized by variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Addition features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum).
Id715625007
StatusPrimitive
Pathological processproces van pathologische ontwikkeling
Interpretsmeetbare observatie betreffende lengte en/of groei
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE34.3
TermKleine gestalte, niet elders geclassificeerd
SNOMED CT to Orphanet simple map73273
SNOMED CT to ICD-10 extended map
TargetE34.3
RuleTRUE
AdviceALWAYS E34.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified