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