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 (2)
MIM:603457 - BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS

Xenbase Genes: smchd1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011323 - arhinia, choanal atresia, and microphthalmia
MONDO:0015238 - arrhinia-choanal atresia-microphthalmia syndrome
MONDO:0016393 - hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome