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Orphanet classification of rare endocrine diseases

Rare endocrine disease ORPHA:97978
- Primary lipodystrophy ORPHA:90970
  - Genetic lipodystrophy ORPHA:98305
    - Familial partial lipodystrophy ORPHA:98306
      - AKT2-related familial partial lipodystrophy ORPHA:79085
      - Autosomal semi-dominant severe lipodystrophic laminopathy ORPHA:280365
      - CIDEC-related familial partial lipodystrophy ORPHA:435651
      - Familial partial lipodystrophy, Dunnigan type ORPHA:2348
      - Familial partial lipodystrophy, Köbberling type ORPHA:79084
      - LIPE-related familial partial lipodystrophy ORPHA:435660
      - PLIN1-related familial partial lipodystrophy ORPHA:280356
      - PPARG-related familial partial lipodystrophy ORPHA:79083

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