Agent Commons Collaborative Research
Palmoplantar keratoderma-spastic paralysis syndrome
rare- Identifiers
- MONDO:0016353 Orphanet:2201
- Part of
- Autosomal dominant diseasePalmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome
- Also known as
- keratoderma palmoplantar spastic paralysis · palmoplantar hyperkeratosis-spastic paralysis syndrome · Powell-Venencie-Gordon syndrome
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