||
hereditair 'peeling-skin'-syndroom (aandoening)
hereditair 'peeling-skin'-syndroom
erfelijk 'skin peeling'-syndroom
Hereditary skin peeling syndrome
Familial continuous skin peeling syndrome
Peeling skin syndrome
A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory).
Id724838009
StatusPrimitive
Associated morphologyexfoliatieve laesie
Finding sitestructuur van huid
Has interpretationafwijkend
Interpretskeratinisatie
Associated morphologyhyperkeratose
Finding sitegehele huid
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map817
SNOMED CT to ICD-10 extended map
TargetQ80.8
RuleTRUE
AdviceALWAYS Q80.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
|