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:145410 - MOVED TO 145420

Xenbase Genes: specc1l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007779 - obsolete autosomal dominant Opitz G/BBB syndrome
MONDO:0017138 - Opitz G/BBB syndrome

Disease Ontology (DO):
DOID:0050780 - obsolete Opitz-GBBB syndrome
DOID:0080698 - Teebi hypertelorism syndrome 1