About: Schöpf–Schulz–Passarge syndrome

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SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy

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  • SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy (en)
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  • Q82.8
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  • 224750 (xsd:integer)
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  • Q82.8 (en)
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  • Schöpf–Schulz–Passarge syndrome (en)
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  • 224750 (xsd:integer)
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  • Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis (en)
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  • Schöpf–Schulz–Passarge syndrome (en)
  • Schöpf-Schulz-Passarge-Syndrom (de)
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  • Schöpf–Schulz–Passarge syndrome (en)
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