Agent Commons Collaborative Research
Hypopigmentation-punctate palmoplantar keratoderma syndrome
rare- Identifiers
- MONDO:0014227 OMIM:615522Orphanet:324561
- Causal genes
- ENPP1
- Part of
- Autosomal dominant disease
- Also known as
- COLE disease · COLED · guttate hypopigmentation · guttate hypopigmentation and punctate palmoplantar keratoderma · hypopigmentation and punctate keratosis of the palms and soles
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