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Orphanet classification of rare skin diseases

Rare skin disease ORPHA:89826
- Metabolic disease with skin involvement ORPHA:79387
  - Congenital disorder of glycosylation with skin involvement ORPHA:371200
    - Autosomal recessive cutis laxa type 2A ORPHA:357058
    - CHIME syndrome ORPHA:3474
    - COG7-CDG ORPHA:79333
    - DK1-CDG ORPHA:91131
    - Dowling-Degos disease ORPHA:79145
    - Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome ORPHA:306661
    - GM3 synthase deficiency ORPHA:370933
    - MPDU1-CDG ORPHA:79323
    - Musculocontractural Ehlers-Danlos syndrome ORPHA:2953
    - PMM2-CDG ORPHA:79318
    - SRD5A3-CDG ORPHA:324737

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