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 form of genetic lipodystrophy with 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. Inherited in an autosomal dominant manner.
Finding sitestructuur van romp
Associated morphologydystrofie
Finding sitestructuur van panniculus adiposus
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermLipodystrofie, niet elders geclassificeerd
SNOMED CT to Orphanet simple map2348
SNOMED CT to ICD-10 extended map
AdviceALWAYS E88.1
CorrelationSNOMED CT source code to target map code correlation not specified