||||||||||||
syndroom van keratosis palmoplantaris met cysteuze oogleden, hypodontie en hypotrichose (aandoening)
syndroom van keratosis palmoplantaris met cysteuze oogleden, hypodontie en hypotrichose
SSPS
Schöpf-Schulz-Passarge-syndroom
syndroom van Schöpf-Schulz-Passarge
Schöpf-Schulz-Passarge syndrome
Palmoplantar hyperkeratosis, cystic eyelids, hypodontia, hypotrichosis syndrome
Palmoplantar keratoderma, cystic eyelids, hypodontia, hypotrichosis syndrome
Schöpf Schulz Passarge syndrome
SSPS - Schöpf Schulz Passarge syndrome
Eccrine tumors ectodermal dysplasia
Keratosis palmoplantaris, cystic eyelids, hypodontia, hypotrichosis syndrome
Id700062000
StatusPrimitive
Associated morphologydysplasie
Finding sitestructuur van ectoderm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologydystrofie
Finding sitestructuur van nagel
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyverandering in groei
Finding sitestructuur van pilus
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyafwijkend aantal
Finding sitestructuur van gebitselement
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyafwezigheid
Finding sitestructuur van gebitselement
Occurrencecongenitaal
Associated morphologymultipele cysten
Finding sitestructuur van palpebra
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ82.8
TermOverige gespecificeerde congenitale misvormingen van huid
SNOMED CT to Orphanet simple map50944
SNOMED CT to ICD-10 extended map
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