neuronal ceroid lipofuscinosis 9

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Summary

Literature (0)

DOID:0110733 - neuronal ceroid lipofuscinosis 9

Disease Ontology Definition:A neuronal ceroid lipofuscinosis that is characterized by juvenile-onset of progressive vision loss, progressive ataxia and seziures.

Synonyms: CLN9,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), neuronal ceroid lipofuscinosis (is_a)