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Orphanet classification of rare skin diseases

Rare skin disease ORPHA:89826
- Autoimmune disease with skin involvement ORPHA:315350
- Dermis disorder ORPHA:79377
- Epidermal appendage anomaly ORPHA:79362
- Epidermal disease ORPHA:79353
- Immune deficiency with skin involvement ORPHA:79391
- Metabolic disease with skin involvement ORPHA:79387
- Other acquired skin disease ORPHA:90077
- Pigmentation anomaly of the skin ORPHA:79374
- Premature aging ORPHA:79389
- Primary lymphedema ORPHA:77240
- Rare photodermatosis ORPHA:79390
- Rare skin tumor or hamartoma ORPHA:79386
- Rare urticaria ORPHA:79384
- Subcutaneous tissue disease ORPHA:79382
- Systemic disease with skin involvement ORPHA:290836
- Toxic dermatosis ORPHA:293815
- Unclassified genetic skin disorder ORPHA:79385

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