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Collaborative Research
Diseases
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Syndromic disease
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Ectodermal dysplasia syndrome
Dermatopathia pigmentosa reticularis
rare
Identifiers
MONDO:0007445
OMIM:125595
Orphanet:86920
Causal genes
KRT14
Part of
Diffuse palmoplantar keratoderma
Ectodermal dysplasia syndrome
Hyperpigmentation of the skin
Also known as
DPR
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