Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616029 - ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME; ECTDS

Xenbase Genes: grhl2

Human Disease Resource: OMIM

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