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:0110725 - neuronal ceroid lipofuscinosis 10

Disease Ontology Definition:A neuronal ceroid lipofuscinosis that has_material_basis_in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15.

Synonyms: Cathepsin D deficiency, CLN10, neuronal ceroid lipofuscinosis cathepsin D-deficient, neuronal ceroid lipofuscinosis due to cathepsin D deficiency

Xenbase Genes : ctsd

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012414 - neuronal ceroid lipofuscinosis 10

MIM:
MIM:610127 - CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal recessive disease (is_a), genetic disease (is_a), neuronal ceroid lipofuscinosis (is_a)