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disease > stomatology > dental disease > Schöpf-Schulz-Passarge syndrome
disease > genetic disease > hereditary disease > Schöpf-Schulz-Passarge syndrome
disease > congenital disease > malformation > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
disease > stomatology > dental disease > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
disease > dysplasia > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
disease > genetic disease > hereditary disease > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
... > disease > skin appendages disease > skin disease > sweat gland disease > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
disease > skin appendages disease > hypotrichosis > ectodermal dysplasia > Schöpf-Schulz-Passarge syndrome
disease > skin appendages disease > skin disease > onychodystrophy > Schöpf-Schulz-Passarge syndrome
disease > skin appendages disease > nail disease > onychodystrophy > Schöpf-Schulz-Passarge syndrome
disease > tumor > benign neoplasm > cyst > Schöpf-Schulz-Passarge syndrome
disease > eye disease > eyelid disease > Schöpf-Schulz-Passarge syndrome
... > disease > skin appendages disease > skin disease > dyskeratosis > hyperkeratosis > keratoderma > keratoderma palmoplantaris > Schöpf-Schulz-Passarge syndrome
disease > skin appendages disease > hypotrichosis > Schöpf-Schulz-Passarge syndrome

Preferred term

Schöpf-Schulz-Passarge syndrome  

Definition(s)

  • Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts (apocrine hidrocystomas). (Wikipedia)

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http://data.loterre.fr/ark:/67375/VH8-KN9CVK4Z-N

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