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Summary Literature (0)
MIM:616029 - ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME; ECTDS

Xenbase Genes: grhl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014460 - nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome