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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Rare genetic diabetes mellitus ORPHA:183625
    - Rare insulin-resistance syndrome ORPHA:181368
      - Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome ORPHA:90301
      - Autosomal semi-dominant severe lipodystrophic laminopathy ORPHA:280365
      - Congenital generalized lipodystrophy ORPHA:528
      - Insulin-resistance syndrome type A ORPHA:2297
      - Insulin-resistance syndrome type B ORPHA:2298
      - Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome ORPHA:436144
      - Leprechaunism ORPHA:508
      - Microcephalic primordial dwarfism-insulin resistance syndrome ORPHA:436182
      - PLIN1-related familial partial lipodystrophy ORPHA:280356
      - Rabson-Mendenhall syndrome ORPHA:769
      - Short fifth metacarpals-insulin resistance syndrome ORPHA:66518
      - SHORT syndrome ORPHA:3163

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