| 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. |
| | Id | 715439000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E88.1 | | Term | Lipodystrofie, niet elders geclassificeerd |
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| SNOMED CT to Orphanet simple map | 2348 |
| SNOMED CT to ICD-10 extended map | | Target | E88.1 | | Rule | TRUE | | Advice | ALWAYS E88.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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