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syndroom van marfanoïde habitus, hernia inguinalis en gevorderde botleeftijd (aandoening)
syndroom van marfanoïde habitus, hernia inguinalis en gevorderde botleeftijd
syndroom van marfanoïde habitus, liesbreuk en gevorderde botleeftijd
Marfanoid habitus, inguinal hernia, advanced bone age syndrome
A very rare developmental defect with connective tissue involvement disorder that has characteristics of tall stature, inguinal hernia, facial dysmorphism (including a long, triangular face, prominent forehead, telecanthus, downslanting palpebral fissures, bilateral ptosis, everted lower eyelids, large ears, long nose, full, everted vermilions, narrow and high arched palate, dental crowding), and radiologic evidence of advanced bone age. Additional manifestations include hyperextensible joints, long digits, mild muscle weakness, myopia, and foot deformities (such as hallux valgus, talipes equinovarus).
Id782780007
StatusPrimitive
Associated morphologyherniatie
Finding sitestructuur van abdomen
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologybreukpoort
Finding sitestructuur van canalis inguinalis
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Interpretslichaamsbouw
referentieset met complexe 'mapping' naar ICD-10
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified