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)
DOID:0110708 - hypotrichosis 11


Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of SNRPE on chromosome 1q32.1.

Synonyms: Hypt11

Xenbase Genes : snrpe

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014027 - hypotrichosis 11

OMIM:
OMIM:615059 - HYPOTRICHOSIS 11; HYPT11

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hypotrichosis (is_a)