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

In OMIM:
OMIM:610127 - CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10

In Mondo Disease Ontology:
MONDO:0012414 - neuronal ceroid lipofuscinosis 10

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

Xenbase Genes : ctsd

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