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syndroom van afwezigheid van dermatoglyfen en congenitale milia (aandoening)
syndroom van afwezigheid van dermatoglyfen en congenitale milia
syndroom van Baird
Baird-syndroom
Absence of fingerprints with congenital milia syndrome
Absence of dermatoglyphics with congenital milia syndrome
Baird syndrome
This syndrome has characteristics of neonatal blisters, milia and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait.
Id719595002
StatusPrimitive
Associated morphologypseudomilium
Finding sitestructuur van huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ82.8
RuleTRUE
AdviceALWAYS Q82.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified