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:0110732 - neuronal ceroid lipofuscinosis 11


Disease Ontology Definition:A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with rapidly progressive visual loss due to retinal dystrophy, seizures, cerebellar ataxia, and cerebellar atrophy and has_material_basis_in homozygous mutation in the GRN gene on chromosome 17q.

Synonyms: CLN11

In OMIM:
OMIM:614706 - CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11

In Mondo Disease Ontology:
MONDO:0013866 - neuronal ceroid lipofuscinosis 11

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : grn

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): genetic disease (is_a), neuronal ceroid lipofuscinosis (is_a)