autosomaal dominante hereditaire aandoening
familiaire partiële lipodystrofie
hereditaire aandoening van bindweefsel
hereditaire aandoening van integumentum
||||
familiaire partiële lipodystrofie type 2 (aandoening)
familiaire partiële lipodystrofie type 2
familiaire partiële lipodystrofie van Dunnigan-type
Familial partial lipodystrophy Dunnigan type
Dunnigan syndrome
Familial partial lipodystrophy type 2
A rare, genetic lipodystrophy characterized by a loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance, diabetes mellitus, dyslipidemia and liver steatosis.
Id715439000
StatusPrimitive
Finding sitestructuur van romp
Finding sitestructuur van extremiteit
Associated morphologydystrofie
Finding sitestructuur van panniculus adiposus
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE88.1
TermLipodystrofie, niet elders geclassificeerd
SNOMED CT to Orphanet simple map2348
SNOMED CT to ICD-10 extended map
TargetE88.1
RuleTRUE
AdviceALWAYS E88.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified