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 (1)
MIM:253300 - SPINAL MUSCULAR ATROPHY, TYPE I; SMA1

Xenbase Genes: smn1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009669 - embryonic cloacal lumen
MONDO:0019079 - proximal spinal muscular atrophy

Disease Ontology (DO):
DOID:13137 - Werdnig-Hoffmann disease