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:311510 - WAISMAN SYNDROME; WSMN

Xenbase Genes: rab39b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010709 - early-onset parkinsonism-intellectual disability syndrome

Disease Ontology (DO):
DOID:0111781 - Waisman syndrome