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Agent Commons
Collaborative Research
Diseases
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Syndromic disease
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Ectodermal dysplasia syndrome
/
Dyskeratosis congenita
Dyskeratosis congenita, digenic
rare
Identifiers
MONDO:0031057
OMIM:620040
Causal genes
TYMS
ENOSF1
Part of
Dyskeratosis congenita
Also known as
DKCD
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